NP-MRD: Showing NP-Card for (2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0144573)

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Record Information

Version

2.0

Created at

2022-09-01 23:34:49 UTC

Updated at

2022-09-01 23:34:49 UTC

NP-MRD ID

NP0144573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(2S,3R,4R,5S,6S)-2-({[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl 3-(3,4-dihydroxyphenyl)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. (2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate is found in Phlomoides rotata. Based on a literature review very few articles have been published on (2S,3R,4R,5S,6S)-2-({[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201342D          

 54 58  0  0  1  0            999 V2000
    3.8328  -12.8939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3479  -12.2265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6834  -11.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1985  -10.8054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5341  -10.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0491   -9.3843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2287   -9.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7437   -8.8031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9232   -8.8893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4383   -8.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3822   -8.3081    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8671   -7.6407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5315   -6.8870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -6.2195    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8414   -6.2195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964   -5.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9810   -4.3369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8769   -4.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0699   -4.5084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -5.4349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0231   -5.1800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7177   -9.0618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5382   -9.1480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0231   -8.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6876   -7.7269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8436   -8.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3285   -7.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1490   -7.9856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4846   -8.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3050   -8.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7900   -8.1581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6104   -8.2443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4544   -7.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9393   -6.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6339   -7.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2328   -9.7292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5683  -10.4829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834  -11.1503    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7371  -11.0641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2220  -11.7315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0425  -11.6453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8864  -12.4852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3713  -13.1526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0659  -12.5714    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2696  -13.3251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4190  -11.9040    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2395  -11.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5877   -9.6430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0726  -10.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3545   -9.9655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395  -10.6329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5039  -11.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9888  -12.0540    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  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  6  0  0  0
 17 19  1  1  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  6  0  0  0
 11 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  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
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 23 37  1  0  0  0  0
 37 38  1  1  0  0  0
 39 38  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 47  1  0  0  0  0
 39 47  1  0  0  0  0
 47 48  1  6  0  0  0
 37 49  1  0  0  0  0
  9 49  1  0  0  0  0
 49 50  1  1  0  0  0
  5 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
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   -4.5709    5.7889    2.8696 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5922    4.4542   -0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5812    1.6505   -1.1572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2118    0.5886   -1.8198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3373   -0.5141   -0.9982 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5987   -1.7471   -1.7673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7323   -2.1441   -2.7252 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621   -1.3748   -3.8346 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8429   -2.1268   -4.9974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4296   -1.3339   -6.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7541   -0.5519   -5.5942 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.4049    1.4259   -6.9190 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8568   -0.9506   -4.1187 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7494   -2.0020   -3.9908 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5178   -2.2678    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
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    4.4700   -2.1057    2.7837 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -4.3553    1.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4771    1.4769   -1.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5407    7.1243   -1.2686 H   0  0  0  0  0  0  0  0  0  0  0  0
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 48 95  1  0
 49 96  1  6
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 51 98  1  0
 52 99  1  0
 54100  1  0
M  END


  Mrv1652309022201342D          

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   -5.7900   -8.1581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6104   -8.2443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9393   -6.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2328   -9.7292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5683  -10.4829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834  -11.1503    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7371  -11.0641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2220  -11.7315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0425  -11.6453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8864  -12.4852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3713  -13.1526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2696  -13.3251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2395  -11.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3545   -9.9655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395  -10.6329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5039  -11.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9888  -12.0540    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
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 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  6  0  0  0
 11 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  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
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 23 37  1  0  0  0  0
 37 38  1  1  0  0  0
 39 38  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 47  1  0  0  0  0
 39 47  1  0  0  0  0
 47 48  1  6  0  0  0
 37 49  1  0  0  0  0
  9 49  1  0  0  0  0
 49 50  1  1  0  0  0
  5 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CCO[C@H]2O[C@@H](CO[C@@H]3OC[C@@](O)(CO)[C@@H]3O)[C@@H](OC(=O)\C=C\C3=CC=C(O)C(O)=C3)[C@H](O[C@H]3O[C@H](C)[C@H](O)[C@H](O)[C@@H]3O)[C@@H]2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H46O19/c1-16-25(41)26(42)27(43)33(51-16)54-30-28(44)32(48-10-9-18-4-7-20(38)22(12-18)47-2)52-23(13-49-34-31(45)35(46,14-36)15-50-34)29(30)53-24(40)8-5-17-3-6-19(37)21(39)11-17/h3-8,11-12,16,23,25-34,36-39,41-46H,9-10,13-15H2,1-2H3/b8-5+/t16-,23+,25+,26+,27+,28+,29-,30-,31-,32+,33-,34-,35+/m1/s1

> <INCHI_KEY>
RXDDCGCFNNKGCJ-BKPFSLNHSA-N

> <FORMULA>
C35H46O19

> <MOLECULAR_WEIGHT>
770.734

> <EXACT_MASS>
770.263329261

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
75.56395968807874

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
0.48

> <JCHEM_LOGP>
-0.3111796436666649

> <ALOGPS_LOGS>
-2.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.21057714384721

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.16341133215085

> <JCHEM_PKA_STRONGEST_BASIC>
-3.676505497283866

> <JCHEM_POLAR_SURFACE_AREA>
293.21

> <JCHEM_REFRACTIVITY>
179.55560000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.26e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       7.155 -24.069   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.249 -22.823   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.876 -21.416   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.971 -20.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.597 -18.763   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.692 -17.517   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.160 -17.678   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.255 -16.432   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.723 -16.593   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.818 -15.347   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.713 -15.508   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.619 -14.263   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.992 -12.856   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.897 -11.610   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.437 -11.610   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.913 -10.145   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.698  -8.096   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.637  -8.096   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.131  -8.416   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.421 -10.145   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.043  -9.669   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.340 -16.915   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.871 -17.076   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.776 -15.830   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.150 -14.424   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.308 -15.991   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.213 -14.745   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.745 -14.906   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.371 -16.313   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.903 -16.474   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -10.808 -15.228   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -12.339 -15.389   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -10.182 -13.822   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -11.087 -12.576   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -8.650 -13.661   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.435 -18.161   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -1.061 -19.568   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -0.156 -20.814   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       1.376 -20.653   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.281 -21.899   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.813 -21.738   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.655 -23.306   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       2.560 -24.552   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       0.123 -23.467   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -0.503 -24.874   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -0.782 -22.221   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -2.314 -22.382   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       1.097 -18.000   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       2.002 -19.246   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       8.128 -18.602   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       9.034 -19.848   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       8.407 -21.255   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       9.312 -22.501   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   53                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   49                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   21                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   17   14   22                                                  
CONECT   22   21                                                            
CONECT   23   11   24   37                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29                                                       
CONECT   37   23   38   49                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   47                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   39   48                                                  
CONECT   48   47                                                            
CONECT   49   37    9   50                                                  
CONECT   50   49                                                            
CONECT   51    5   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52    3   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  116    0
END

View in JSmol

Synonyms

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

Chemical Formula

C₃₅H₄₆O₁₉

Average Mass

770.7340 Da

Monoisotopic Mass

770.26333 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(CCO[C@H]2O[C@@H](CO[C@@H]3OC[C@@](O)(CO)[C@@H]3O)[C@@H](OC(=O)\C=C\C3=CC=C(O)C(O)=C3)[C@H](O[C@H]3O[C@H](C)[C@H](O)[C@H](O)[C@@H]3O)[C@@H]2O)=CC=C1O

InChI Identifier

InChI=1S/C35H46O19/c1-16-25(41)26(42)27(43)33(51-16)54-30-28(44)32(48-10-9-18-4-7-20(38)22(12-18)47-2)52-23(13-49-34-31(45)35(46,14-36)15-50-34)29(30)53-24(40)8-5-17-3-6-19(37)21(39)11-17/h3-8,11-12,16,23,25-34,36-39,41-46H,9-10,13-15H2,1-2H3/b8-5+/t16-,23+,25+,26+,27+,28+,29-,30-,31-,32+,33-,34-,35+/m1/s1

InChI Key

RXDDCGCFNNKGCJ-BKPFSLNHSA-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
Lamiophlomis rotata	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
Anisole
Catechol
Phenoxy compound
Methoxybenzene
Phenol ether
Styrene
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Monocyclic benzene moiety
Benzenoid
Oxane
Fatty acyl
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Acetal
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	0.48	ALOGPS
logP	-0.31	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	9.16	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	293.21 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	179.56 m³·mol⁻¹	ChemAxon
Polarizability	75.56 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

163195437

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0144573)

MOL for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D MOL for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D SDF for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D-SDF for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

PDB for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D PDB for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

SMILES for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

INCHI for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

Structure for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D Structure for NP0144573 ((2s,3r,4r,5s,6s)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-4-{[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)