Hmdb loader

Showing metabocard for 6-C-Fucosylluteolin (HMDB0038898)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 00:14:47 UTC
Update Date2022-03-07 02:55:59 UTC
HMDB IDHMDB0038898
Secondary Accession Numbers
  • HMDB38898
Metabolite Identification
Common Name6-C-Fucosylluteolin
Description6-C-Fucosylluteolin belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. 6-C-Fucosylluteolin has been detected, but not quantified in, fruits and passion fruits (Passiflora edulis). This could make 6-C-fucosylluteolin a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 6-C-Fucosylluteolin.
Structure
Data?1563863277
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0038898 (6-C-Fucosylluteolin)


  Mrv0541 05061311262D          

 31 34  0  0  0  0            999 V2000
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  0  0  0  0
  8  4  2  0  0  0  0
  9  3  1  0  0  0  0
 10  4  1  0  0  0  0
 10  9  2  0  0  0  0
 11  5  1  0  0  0  0
 12  6  2  0  0  0  0
 13  5  2  0  0  0  0
 13  8  1  0  0  0  0
 14  6  1  0  0  0  0
 15 11  1  0  0  0  0
 15 14  2  0  0  0  0
 16 12  1  0  0  0  0
 17  7  1  0  0  0  0
 18 15  1  0  0  0  0
 18 16  2  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 25 12  1  0  0  0  0
 26 17  1  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 21  1  0  0  0  0
 31 13  1  0  0  0  0
 31 14  1  0  0  0  0
M  END
Download

3D MOL for HMDB0038898 (6-C-Fucosylluteolin)

HMDB0038898
     RDKit          3D
6-C-Fucosylluteolin
 51 54  0  0  0  0  0  0  0  0999 V2000
   -5.0477    2.1410   -1.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4081    0.7825   -1.0635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5259    0.8832   -0.0316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9714   -0.3238    0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5113   -0.1806    0.4108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9778    0.8841    1.1634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8624    1.7061    1.8333 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3500    1.1128    1.2416 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2030    0.2655    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806    0.5323    0.6650 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4011   -0.1677    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7949    0.2089    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1298    1.3073    1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4436    1.6431    1.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4825    0.9469    0.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7878    1.3382    0.8271 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1661   -0.1350   -0.1539 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1749   -0.8699   -0.7696 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8256   -0.4888   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -1.2350   -0.6814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6668   -1.5563   -0.8274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -2.5268   -1.5246 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7240   -0.7873   -0.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6555   -1.0381   -0.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1187   -2.0670   -1.0155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5105   -1.5057   -0.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1389   -2.6671    0.4215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0416   -1.4503   -0.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2880   -1.3049    1.2301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233   -0.2069   -0.8241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5821    0.3977   -0.1411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    2.6000   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3588    2.8309   -1.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0353    2.0784   -1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9177    0.5061   -2.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3242   -0.3991    1.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5009    2.4710    2.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7376    1.9399    1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3395    1.8726    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7012    2.5016    1.8360 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5421    0.8189    0.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9264   -1.6623   -1.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6584   -1.3435   -0.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7289   -1.8376   -1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7592   -2.7569   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2739   -1.6456   -1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8230   -2.4267    1.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4887   -2.3789   -0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5378   -0.3811    1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9170   -0.5050   -1.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3580   -0.2266   -0.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 11 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
  4 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30  2  1  0
 24  5  1  0
 23  9  1  0
 19 12  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  4 36  1  0
  7 37  1  0
  8 38  1  0
 13 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 20 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 28 48  1  0
 29 49  1  0
 30 50  1  0
 31 51  1  0
M  END
Download

3D SDF for HMDB0038898 (6-C-Fucosylluteolin)


  Mrv0541 05061311262D          

 31 34  0  0  0  0            999 V2000
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  0  0  0  0
  8  4  2  0  0  0  0
  9  3  1  0  0  0  0
 10  4  1  0  0  0  0
 10  9  2  0  0  0  0
 11  5  1  0  0  0  0
 12  6  2  0  0  0  0
 13  5  2  0  0  0  0
 13  8  1  0  0  0  0
 14  6  1  0  0  0  0
 15 11  1  0  0  0  0
 15 14  2  0  0  0  0
 16 12  1  0  0  0  0
 17  7  1  0  0  0  0
 18 15  1  0  0  0  0
 18 16  2  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 25 12  1  0  0  0  0
 26 17  1  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 21  1  0  0  0  0
 31 13  1  0  0  0  0
 31 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038898

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O10/c1-7-17(26)19(28)20(29)21(30-7)16-12(25)6-14-15(18(16)27)11(24)5-13(31-14)8-2-3-9(22)10(23)4-8/h2-7,17,19-23,25-29H,1H3

> <INCHI_KEY>
ROQHTXBYBLROKW-UHFFFAOYSA-N

> <FORMULA>
C21H20O10

> <MOLECULAR_WEIGHT>
432.3775

> <EXACT_MASS>
432.10564686

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
42.61425068461187

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)-4H-chromen-4-one

> <ALOGPS_LOGP>
1.12

> <JCHEM_LOGP>
0.692712873666667

> <ALOGPS_LOGS>
-2.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.489548156917554

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.196627616525169

> <JCHEM_PKA_STRONGEST_BASIC>
-3.608542600863829

> <JCHEM_POLAR_SURFACE_AREA>
177.14

> <JCHEM_REFRACTIVITY>
106.46939999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.59e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0038898 (6-C-Fucosylluteolin)

HMDB0038898
     RDKit          3D
6-C-Fucosylluteolin
 51 54  0  0  0  0  0  0  0  0999 V2000
   -5.0477    2.1410   -1.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4081    0.7825   -1.0635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5259    0.8832   -0.0316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9714   -0.3238    0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5113   -0.1806    0.4108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9778    0.8841    1.1634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8624    1.7061    1.8333 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3500    1.1128    1.2416 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2030    0.2655    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4806    0.5323    0.6650 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4011   -0.1677    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7949    0.2089    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1298    1.3073    1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4436    1.6431    1.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4825    0.9469    0.6273 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7878    1.3382    0.8271 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1661   -0.1350   -0.1539 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1749   -0.8699   -0.7696 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8256   -0.4888   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -1.2350   -0.6814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6668   -1.5563   -0.8274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -2.5268   -1.5246 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7240   -0.7873   -0.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6555   -1.0381   -0.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1187   -2.0670   -1.0155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5105   -1.5057   -0.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1389   -2.6671    0.4215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0416   -1.4503   -0.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2880   -1.3049    1.2301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233   -0.2069   -0.8241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5821    0.3977   -0.1411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    2.6000   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3588    2.8309   -1.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0353    2.0784   -1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9177    0.5061   -2.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3242   -0.3991    1.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5009    2.4710    2.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7376    1.9399    1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3395    1.8726    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7012    2.5016    1.8360 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5421    0.8189    0.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9264   -1.6623   -1.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6584   -1.3435   -0.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7289   -1.8376   -1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7592   -2.7569   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2739   -1.6456   -1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8230   -2.4267    1.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4887   -2.3789   -0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5378   -0.3811    1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9170   -0.5050   -1.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3580   -0.2266   -0.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 11 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
  4 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30  2  1  0
 24  5  1  0
 23  9  1  0
 19 12  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  4 36  1  0
  7 37  1  0
  8 38  1  0
 13 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 20 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 28 48  1  0
 29 49  1  0
 30 50  1  0
 31 51  1  0
M  END
Download

PDB for HMDB0038898 (6-C-Fucosylluteolin)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.336   6.930   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       6.668   8.470   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2    3    8                                                       
CONECT    3    2    9                                                       
CONECT    4    8   10                                                       
CONECT    5   11   13                                                       
CONECT    6   12   14                                                       
CONECT    7    1   17   30                                                  
CONECT    8    2    4   13                                                  
CONECT    9    3   10   22                                                  
CONECT   10    4    9   23                                                  
CONECT   11    5   15   24                                                  
CONECT   12    6   16   25                                                  
CONECT   13    5    8   31                                                  
CONECT   14    6   15   31                                                  
CONECT   15   11   14   18                                                  
CONECT   16   12   18   21                                                  
CONECT   17    7   19   26                                                  
CONECT   18   15   16   27                                                  
CONECT   19   17   20   28                                                  
CONECT   20   19   21   29                                                  
CONECT   21   16   20   30                                                  
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   17                                                            
CONECT   27   18                                                            
CONECT   28   19                                                            
CONECT   29   20                                                            
CONECT   30    7   21                                                       
CONECT   31   13   14                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END
Download

3D PDB for HMDB0038898 (6-C-Fucosylluteolin)

COMPND    HMDB0038898
HETATM    1  C1  UNL     1      -5.048   2.141  -1.263  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.408   0.783  -1.063  1.00  0.00           C  
HETATM    3  O1  UNL     1      -3.526   0.883  -0.032  1.00  0.00           O  
HETATM    4  C3  UNL     1      -2.971  -0.324   0.400  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.511  -0.181   0.411  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.978   0.884   1.163  1.00  0.00           C  
HETATM    7  O2  UNL     1      -1.862   1.706   1.833  1.00  0.00           O  
HETATM    8  C6  UNL     1       0.350   1.113   1.242  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.203   0.266   0.555  1.00  0.00           C  
HETATM   10  O3  UNL     1       2.481   0.532   0.665  1.00  0.00           O  
HETATM   11  C8  UNL     1       3.401  -0.168   0.083  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.795   0.209   0.266  1.00  0.00           C  
HETATM   13  C10 UNL     1       5.130   1.307   1.058  1.00  0.00           C  
HETATM   14  C11 UNL     1       6.444   1.643   1.216  1.00  0.00           C  
HETATM   15  C12 UNL     1       7.482   0.947   0.627  1.00  0.00           C  
HETATM   16  O4  UNL     1       8.788   1.338   0.827  1.00  0.00           O  
HETATM   17  C13 UNL     1       7.166  -0.135  -0.154  1.00  0.00           C  
HETATM   18  O5  UNL     1       8.175  -0.870  -0.770  1.00  0.00           O  
HETATM   19  C14 UNL     1       5.826  -0.489  -0.323  1.00  0.00           C  
HETATM   20  C15 UNL     1       3.008  -1.235  -0.681  1.00  0.00           C  
HETATM   21  C16 UNL     1       1.667  -1.556  -0.827  1.00  0.00           C  
HETATM   22  O6  UNL     1       1.343  -2.527  -1.525  1.00  0.00           O  
HETATM   23  C17 UNL     1       0.724  -0.787  -0.192  1.00  0.00           C  
HETATM   24  C18 UNL     1      -0.656  -1.038  -0.284  1.00  0.00           C  
HETATM   25  O7  UNL     1      -1.119  -2.067  -1.015  1.00  0.00           O  
HETATM   26  C19 UNL     1      -3.511  -1.506  -0.292  1.00  0.00           C  
HETATM   27  O8  UNL     1      -3.139  -2.667   0.422  1.00  0.00           O  
HETATM   28  C20 UNL     1      -5.042  -1.450  -0.127  1.00  0.00           C  
HETATM   29  O9  UNL     1      -5.288  -1.305   1.230  1.00  0.00           O  
HETATM   30  C21 UNL     1      -5.523  -0.207  -0.824  1.00  0.00           C  
HETATM   31  O10 UNL     1      -6.582   0.398  -0.141  1.00  0.00           O  
HETATM   32  H1  UNL     1      -5.158   2.600  -0.257  1.00  0.00           H  
HETATM   33  H2  UNL     1      -4.359   2.831  -1.827  1.00  0.00           H  
HETATM   34  H3  UNL     1      -6.035   2.078  -1.764  1.00  0.00           H  
HETATM   35  H4  UNL     1      -3.918   0.506  -2.016  1.00  0.00           H  
HETATM   36  H5  UNL     1      -3.324  -0.399   1.482  1.00  0.00           H  
HETATM   37  H6  UNL     1      -1.501   2.471   2.375  1.00  0.00           H  
HETATM   38  H7  UNL     1       0.738   1.940   1.828  1.00  0.00           H  
HETATM   39  H8  UNL     1       4.339   1.873   1.533  1.00  0.00           H  
HETATM   40  H9  UNL     1       6.701   2.502   1.836  1.00  0.00           H  
HETATM   41  H10 UNL     1       9.542   0.819   0.389  1.00  0.00           H  
HETATM   42  H11 UNL     1       7.926  -1.662  -1.341  1.00  0.00           H  
HETATM   43  H12 UNL     1       5.658  -1.344  -0.946  1.00  0.00           H  
HETATM   44  H13 UNL     1       3.729  -1.838  -1.178  1.00  0.00           H  
HETATM   45  H14 UNL     1      -0.759  -2.757  -1.550  1.00  0.00           H  
HETATM   46  H15 UNL     1      -3.274  -1.646  -1.342  1.00  0.00           H  
HETATM   47  H16 UNL     1      -2.823  -2.427   1.331  1.00  0.00           H  
HETATM   48  H17 UNL     1      -5.489  -2.379  -0.472  1.00  0.00           H  
HETATM   49  H18 UNL     1      -5.538  -0.381   1.453  1.00  0.00           H  
HETATM   50  H19 UNL     1      -5.917  -0.505  -1.816  1.00  0.00           H  
HETATM   51  H20 UNL     1      -7.358  -0.227  -0.202  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3   30   35
CONECT    3    4
CONECT    4    5   26   36
CONECT    5    6    6   24
CONECT    6    7    8
CONECT    7   37
CONECT    8    9    9   38
CONECT    9   10   23
CONECT   10   11
CONECT   11   12   20   20
CONECT   12   13   13   19
CONECT   13   14   39
CONECT   14   15   15   40
CONECT   15   16   17
CONECT   16   41
CONECT   17   18   19   19
CONECT   18   42
CONECT   19   43
CONECT   20   21   44
CONECT   21   22   22   23
CONECT   23   24   24
CONECT   24   25
CONECT   25   45
CONECT   26   27   28   46
CONECT   27   47
CONECT   28   29   30   48
CONECT   29   49
CONECT   30   31   50
CONECT   31   51
END
Download

SMILES for HMDB0038898 (6-C-Fucosylluteolin)

CC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O
Download

INCHI for HMDB0038898 (6-C-Fucosylluteolin)

InChI=1S/C21H20O10/c1-7-17(26)19(28)20(29)21(30-7)16-12(25)6-14-15(18(16)27)11(24)5-13(31-14)8-2-3-9(22)10(23)4-8/h2-7,17,19-23,25-29H,1H3
Download
View in JSmolView Stereo Labels
SynonymsNot Available
Chemical FormulaC21H20O10
Average Molecular Weight432.3775
Monoisotopic Molecular Weight432.10564686
IUPAC Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)-4H-chromen-4-one
Traditional Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)chromen-4-one
CAS Registry NumberNot Available
SMILES
CC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O
InChI Identifier
InChI=1S/C21H20O10/c1-7-17(26)19(28)20(29)21(30-7)16-12(25)6-14-15(18(16)27)11(24)5-13(31-14)8-2-3-9(22)10(23)4-8/h2-7,17,19-23,25-29H,1H3
InChI KeyROQHTXBYBLROKW-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid C-glycosides
Alternative Parents
Substituents
  • Flavonoid c-glycoside
  • 3'-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Phenolic glycoside
  • Chromone
  • Benzopyran
  • 1-benzopyran
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Pyranone
  • Oxane
  • Pyran
  • Benzenoid
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Heteroaromatic compound
  • Secondary alcohol
  • Polyol
  • Organoheterocyclic compound
  • Ether
  • Oxacycle
  • Dialkyl ether
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Alcohol
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.59 g/LALOGPS
logP1.12ALOGPS
logP0.69ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)6.2ChemAxon
pKa (Strongest Basic)-3.6ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area177.14 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity106.47 m³·mol⁻¹ChemAxon
Polarizability42.61 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+192.60830932474
DeepCCS[M-H]-190.21330932474
DeepCCS[M-2H]-223.230932474
DeepCCS[M+Na]+198.52130932474
AllCCS[M+H]+204.432859911
AllCCS[M+H-H2O]+201.732859911
AllCCS[M+NH4]+206.932859911
AllCCS[M+Na]+207.632859911
AllCCS[M-H]-201.932859911
AllCCS[M+Na-2H]-202.632859911
AllCCS[M+HCOO]-203.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
6-C-FucosylluteolinCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O5746.2Standard polar33892256
6-C-FucosylluteolinCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O3637.0Standard non polar33892256
6-C-FucosylluteolinCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(=CC2=O)C2=CC(O)=C(O)C=C2)C=C1O4339.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
6-C-Fucosylluteolin,1TMS,isomer #1CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4266.5Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #2CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4297.4Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #3CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4295.9Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #4CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4244.9Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #5CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4298.0Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4302.3Semi standard non polar33892256
6-C-Fucosylluteolin,1TMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4274.9Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4210.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #10CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4171.4Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4216.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #12CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4216.0Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4226.7Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4194.4Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4180.9Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #16CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4248.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #17CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4251.2Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #18CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4229.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #19CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4251.7Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #2CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4211.1Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4224.1Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #21CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4268.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #3CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4185.5Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #4CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4165.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #5CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4200.1Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4218.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4213.0Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #8CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4211.7Semi standard non polar33892256
6-C-Fucosylluteolin,2TMS,isomer #9CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4180.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4056.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #10CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4002.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4037.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #12CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4062.3Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4033.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4057.2Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4115.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #16CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4064.7Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #17CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4042.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #18CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4058.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #19CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4089.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4040.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4063.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #21CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4020.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #22CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4089.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #23CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3991.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #24CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4064.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #25CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4051.3Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #26CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4076.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #27CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4058.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #28CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4091.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #29CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4094.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4088.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #30CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4040.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #31CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4015.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #32CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4141.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #33CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4124.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #34CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4084.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #35CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4123.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4069.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4091.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4078.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #7CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4026.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #8CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4061.3Semi standard non polar33892256
6-C-Fucosylluteolin,3TMS,isomer #9CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4087.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3964.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #10CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4017.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3926.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #12CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3971.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3988.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3880.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3893.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #16CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3989.8Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #17CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3858.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #18CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3866.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #19CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3969.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3954.8Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3983.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #21CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3952.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #22CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4001.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #23CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3941.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #24CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3974.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #25CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3918.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #26CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3975.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #27CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3910.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #28CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3996.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #29CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3910.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3920.5Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #30CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3889.9Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #31CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3971.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #32CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3966.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #33CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3946.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #34CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3938.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #35CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4028.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3938.8Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3935.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #6CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3897.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3912.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #8CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3953.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TMS,isomer #9CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3983.6Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3912.1Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #10CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3900.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3850.1Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #12CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3853.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3960.8Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3857.7Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3839.2Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #16CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3951.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #17CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3904.3Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #18CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3913.9Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #19CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3886.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3886.3Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3877.3Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #21CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3916.9Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3893.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3891.1Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3902.2Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #6CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3892.8Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3862.0Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #8CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3873.5Semi standard non polar33892256
6-C-Fucosylluteolin,5TMS,isomer #9CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3872.2Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3850.7Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3876.2Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3893.1Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3857.1Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3838.3Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3860.7Semi standard non polar33892256
6-C-Fucosylluteolin,6TMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3873.7Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #1CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4554.7Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #2CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4572.8Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #3CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4562.5Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #4CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4507.3Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #5CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4530.5Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4539.1Semi standard non polar33892256
6-C-Fucosylluteolin,1TBDMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4509.2Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4719.0Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #10CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4697.2Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4740.5Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #12CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4729.3Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4731.4Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4697.9Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4713.4Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #16CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4721.4Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #17CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4721.7Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #18CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4695.2Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #19CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4711.7Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #2CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4727.1Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4690.1Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #21CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4734.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #3CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4696.5Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #4CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4703.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #5CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4739.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4758.8Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4719.6Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #8CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4723.0Semi standard non polar33892256
6-C-Fucosylluteolin,2TBDMS,isomer #9CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4689.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4815.7Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #10CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4725.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4740.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #12CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4765.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4733.7Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4765.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4802.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #16CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4832.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #17CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4791.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #18CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4774.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #19CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4777.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4777.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4769.5Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #21CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4775.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #22CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4770.2Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #23CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4733.3Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #24CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4742.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #25CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4744.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #26CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4816.4Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #27CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4781.3Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #28CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4782.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #29CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4783.2Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4789.2Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #30CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4771.6Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #31CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4732.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #32CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4868.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #33CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4830.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #34CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4797.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #35CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O4854.8Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4773.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4803.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #6CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4791.9Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #7CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4770.0Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #8CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4771.1Semi standard non polar33892256
6-C-Fucosylluteolin,3TBDMS,isomer #9CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4800.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #1CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4878.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #10CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4852.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #11CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4795.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #12CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4826.5Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #13CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4849.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #14CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4795.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #15CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4808.9Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #16CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4838.5Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #17CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4751.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #18CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4764.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #19CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4809.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #2CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4890.8Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #20CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4797.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #21CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4887.5Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #22CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4939.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #23CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4886.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #24CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4885.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #25CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4848.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #26CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4802.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #27CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4807.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #28CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4825.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #29CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4815.9Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #3CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4872.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #30CC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4773.5Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #31CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4876.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #32CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4892.1Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #33CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4842.7Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #34CC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4802.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #35CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4921.6Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #4CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4885.0Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #5CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4840.8Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #6CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4833.2Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #7CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4843.4Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #8CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4793.3Semi standard non polar33892256
6-C-Fucosylluteolin,4TBDMS,isomer #9CC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4820.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 6-C-Fucosylluteolin GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-8079400000-78a0a95ffbcce34d042b2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-C-Fucosylluteolin GC-MS (3 TMS) - 70eV, Positivesplash10-0540-9000378000-e3acdf68540c77d8d2022017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-C-Fucosylluteolin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 10V, Positive-QTOFsplash10-001i-0001900000-f164eeac500d20f772242016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 20V, Positive-QTOFsplash10-00l2-2523900000-535bc5b12b061ea6d6602016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 40V, Positive-QTOFsplash10-05mt-6397300000-5488ecec62497839b3332016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 10V, Negative-QTOFsplash10-001i-1013900000-4830861a29f752787e5c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 20V, Negative-QTOFsplash10-01sr-3139700000-811f87744329c358d4682016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 40V, Negative-QTOFsplash10-052o-9473000000-e16cf8f0d4a88efb528a2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 10V, Positive-QTOFsplash10-001i-0000900000-509ee28ef47ce2bd195a2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 20V, Positive-QTOFsplash10-001i-0000900000-509ee28ef47ce2bd195a2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 40V, Positive-QTOFsplash10-0012-0595700000-176802353fbbaee0485c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 10V, Negative-QTOFsplash10-001i-0000900000-96b50b9840c4a64e416b2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 20V, Negative-QTOFsplash10-001i-0000900000-9eea965addbce350e5032021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-C-Fucosylluteolin 40V, Negative-QTOFsplash10-0fba-0791200000-90969861491664a032fb2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB019512
KNApSAcK IDC00006106
Chemspider ID35014688
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound74977561
PDB IDNot Available
ChEBI ID176089
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .