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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-08-27 19:59:31 UTC

Update Date

2022-09-22 18:34:34 UTC

HMDB ID

HMDB0242167

Secondary Accession Numbers

None

Metabolite Identification

Common Name

5-(Galactosylhydroxy)-L-Lysine

Description

5-(Galactosylhydroxy)-L-Lysine, also known as hydroxylysine-galactose or beta-1-galactosyl-O-hydroxylysine, belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Based on a literature review very few articles have been published on 5-(Galactosylhydroxy)-L-Lysine.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv1652308272122092D          

 29 29  0  0  1  0            999 V2000
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  1  0  0  0  0
  5  3  1  0  0  0  0
  6  2  1  0  0  0  0
  7  4  1  1  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 13  3  1  0  0  0  0
  6 14  1  1  0  0  0
 15  4  1  0  0  0  0
  8 16  1  1  0  0  0
  9 17  1  6  0  0  0
 10 18  1  6  0  0  0
 19 11  2  0  0  0  0
 20 11  1  0  0  0  0
 21  5  1  0  0  0  0
 21 12  1  0  0  0  0
 22  7  1  0  0  0  0
 22 12  1  0  0  0  0
 23  5  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  6  0  0  0
  8 26  1  6  0  0  0
  9 27  1  6  0  0  0
 10 28  1  1  0  0  0
 29 12  1  0  0  0  0
M  END

HMDB0242167
     RDKit          3D
5-(Galactosylhydroxy)-L-Lysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    1.4462    0.2654    2.9011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2068    1.3298    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    0.9062    0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3272    0.4064   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9385   -0.7925    0.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2041   -1.2420   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2097   -0.2034   -0.1331 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9363   -1.6206   -1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -2.5204   -1.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -1.0391   -2.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0002    0.0250    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0628    0.4898   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527    0.5660    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2721    0.7699   -0.4610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5120    1.3546    0.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2700    2.5851    0.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6450   -0.5627   -1.0597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4699   -1.2058   -0.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685   -1.3626   -1.2067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1346   -2.0182   -0.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -0.4072   -1.4631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3999    0.3256   -2.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7986   -0.5266    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103    0.6495    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585    1.8320    2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0490    2.0484    2.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065    1.8539   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1077    0.2026   -1.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.2420   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2223   -1.6381    0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.6389    1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6039   -2.1226    0.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1503    0.4153    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1350   -0.6609   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -0.0387   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8848    1.5270   -0.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    1.4887   -1.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9325    0.6787    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3044    1.4953   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7526    3.3127    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387   -0.4861   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -1.0394   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683   -2.0523   -2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -2.3975    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3198   -1.0422   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.1522   -3.2998 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  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
  3 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 10 35  1  0
 12 36  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  6
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END

  Mrv1652308272122092D          

 29 29  0  0  1  0            999 V2000
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    6.6000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  1  0  0  0  0
  5  3  1  0  0  0  0
  6  2  1  0  0  0  0
  7  4  1  1  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 13  3  1  0  0  0  0
  6 14  1  1  0  0  0
 15  4  1  0  0  0  0
  8 16  1  1  0  0  0
  9 17  1  6  0  0  0
 10 18  1  6  0  0  0
 19 11  2  0  0  0  0
 20 11  1  0  0  0  0
 21  5  1  0  0  0  0
 21 12  1  0  0  0  0
 22  7  1  0  0  0  0
 22 12  1  0  0  0  0
 23  5  1  0  0  0  0
  6 24  1  1  0  0  0
  7 25  1  6  0  0  0
  8 26  1  6  0  0  0
  9 27  1  6  0  0  0
 10 28  1  1  0  0  0
 29 12  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242167

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H24N2O8/c13-3-5(1-2-6(14)11(19)20)21-12-10(18)9(17)8(16)7(4-15)22-12/h5-10,12,15-18H,1-4,13-14H2,(H,19,20)/t5?,6-,7+,8-,9-,10+,12?/m0/s1

> <INCHI_KEY>
OWGKYELXGFKIHH-KVUIFDSDSA-N

> <FORMULA>
C12H24N2O8

> <MOLECULAR_WEIGHT>
324.33

> <EXACT_MASS>
324.153265741

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.689491657831798

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

> <ALOGPS_LOGP>
-3.70

> <JCHEM_LOGP>
-6.252708126450762

> <ALOGPS_LOGS>
-0.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.212034819993672

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.848324006648749

> <JCHEM_PKA_STRONGEST_BASIC>
9.801690439238888

> <JCHEM_POLAR_SURFACE_AREA>
188.71999999999997

> <JCHEM_REFRACTIVITY>
71.5843

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.04e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242167
     RDKit          3D
5-(Galactosylhydroxy)-L-Lysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    1.4462    0.2654    2.9011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2068    1.3298    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    0.9062    0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3272    0.4064   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9385   -0.7925    0.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2041   -1.2420   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2097   -0.2034   -0.1331 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9363   -1.6206   -1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -2.5204   -1.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -1.0391   -2.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0002    0.0250    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0628    0.4898   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527    0.5660    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2721    0.7699   -0.4610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5120    1.3546    0.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2700    2.5851    0.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6450   -0.5627   -1.0597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4699   -1.2058   -0.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685   -1.3626   -1.2067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1346   -2.0182   -0.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -0.4072   -1.4631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3999    0.3256   -2.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7986   -0.5266    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103    0.6495    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585    1.8320    2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0490    2.0484    2.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065    1.8539   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1077    0.2026   -1.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.2420   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2223   -1.6381    0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.6389    1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6039   -2.1226    0.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1503    0.4153    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1350   -0.6609   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -0.0387   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8848    1.5270   -0.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    1.4887   -1.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9325    0.6787    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3044    1.4953   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7526    3.3127    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387   -0.4861   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -1.0394   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683   -2.0523   -2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -2.3975    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3198   -1.0422   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.1522   -3.2998 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  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
  3 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 10 35  1  0
 12 36  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  6
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END

HEADER    PROTEIN                                 27-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-AUG-21         0                                  
HETATM    1  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670   8.470   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337   9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337  10.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003  11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       6.668  11.550   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       4.001   6.930   0.000  0.00  0.00           N+0
HETATM   15  O   UNK     0      16.004   9.240   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      14.670  11.550   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      12.003  13.090   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.336  11.550   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.667  10.780   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.336   8.470   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.003   8.470   0.000  0.00  0.00           O+0
HETATM   23  H   UNK     0       6.668  10.010   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.001  10.010   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0      14.670  10.010   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0      13.337  12.320   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      12.003  10.010   0.000  0.00  0.00           H+0
HETATM   28  H   UNK     0      10.669  12.320   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0       9.336  10.010   0.000  0.00  0.00           H+0
CONECT    1    2    5                                                       
CONECT    2    1    6                                                       
CONECT    3    5   13                                                       
CONECT    4    7   15                                                       
CONECT    5    1    3   21   23                                             
CONECT    6    2   11   14   24                                             
CONECT    7    4    8   22   25                                             
CONECT    8    7    9   16   26                                             
CONECT    9    8   10   17   27                                             
CONECT   10    9   12   18   28                                             
CONECT   11    6   19   20                                                  
CONECT   12   10   21   22   29                                             
CONECT   13    3                                                            
CONECT   14    6                                                            
CONECT   15    4                                                            
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   10                                                            
CONECT   19   11                                                            
CONECT   20   11                                                            
CONECT   21    5   12                                                       
CONECT   22    7   12                                                       
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   12                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

COMPND    HMDB0242167
HETATM    1  N1  UNL     1       1.446   0.265   2.901  1.00  0.00           N  
HETATM    2  C1  UNL     1       1.207   1.330   1.978  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.065   0.906   0.552  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.327   0.406  -0.084  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.939  -0.792   0.578  1.00  0.00           C  
HETATM    6  C5  UNL     1       4.204  -1.242  -0.125  1.00  0.00           C  
HETATM    7  N2  UNL     1       5.210  -0.203  -0.133  1.00  0.00           N  
HETATM    8  C6  UNL     1       3.936  -1.621  -1.529  1.00  0.00           C  
HETATM    9  O1  UNL     1       3.084  -2.520  -1.792  1.00  0.00           O  
HETATM   10  O2  UNL     1       4.575  -1.039  -2.619  1.00  0.00           O  
HETATM   11  O3  UNL     1      -0.000   0.025   0.466  1.00  0.00           O  
HETATM   12  C7  UNL     1      -1.063   0.490  -0.254  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.253   0.566   0.457  1.00  0.00           O  
HETATM   14  C8  UNL     1      -3.272   0.770  -0.461  1.00  0.00           C  
HETATM   15  C9  UNL     1      -4.512   1.355   0.176  1.00  0.00           C  
HETATM   16  O5  UNL     1      -4.270   2.585   0.772  1.00  0.00           O  
HETATM   17  C10 UNL     1      -3.645  -0.563  -1.060  1.00  0.00           C  
HETATM   18  O6  UNL     1      -4.470  -1.206  -0.119  1.00  0.00           O  
HETATM   19  C11 UNL     1      -2.368  -1.363  -1.207  1.00  0.00           C  
HETATM   20  O7  UNL     1      -2.135  -2.018  -0.015  1.00  0.00           O  
HETATM   21  C12 UNL     1      -1.240  -0.407  -1.463  1.00  0.00           C  
HETATM   22  O8  UNL     1      -1.400   0.326  -2.631  1.00  0.00           O  
HETATM   23  H1  UNL     1       0.799  -0.527   2.846  1.00  0.00           H  
HETATM   24  H2  UNL     1       1.610   0.650   3.836  1.00  0.00           H  
HETATM   25  H3  UNL     1       0.259   1.832   2.291  1.00  0.00           H  
HETATM   26  H4  UNL     1       2.049   2.048   2.059  1.00  0.00           H  
HETATM   27  H5  UNL     1       0.807   1.854  -0.017  1.00  0.00           H  
HETATM   28  H6  UNL     1       2.108   0.203  -1.150  1.00  0.00           H  
HETATM   29  H7  UNL     1       3.062   1.242  -0.085  1.00  0.00           H  
HETATM   30  H8  UNL     1       2.222  -1.638   0.524  1.00  0.00           H  
HETATM   31  H9  UNL     1       3.204  -0.639   1.623  1.00  0.00           H  
HETATM   32  H10 UNL     1       4.604  -2.123   0.406  1.00  0.00           H  
HETATM   33  H11 UNL     1       5.150   0.415   0.712  1.00  0.00           H  
HETATM   34  H12 UNL     1       6.135  -0.661  -0.210  1.00  0.00           H  
HETATM   35  H13 UNL     1       4.644  -0.039  -2.696  1.00  0.00           H  
HETATM   36  H14 UNL     1      -0.885   1.527  -0.660  1.00  0.00           H  
HETATM   37  H15 UNL     1      -2.914   1.489  -1.226  1.00  0.00           H  
HETATM   38  H16 UNL     1      -4.933   0.679   0.948  1.00  0.00           H  
HETATM   39  H17 UNL     1      -5.304   1.495  -0.587  1.00  0.00           H  
HETATM   40  H18 UNL     1      -4.753   3.313   0.305  1.00  0.00           H  
HETATM   41  H19 UNL     1      -4.139  -0.486  -2.030  1.00  0.00           H  
HETATM   42  H20 UNL     1      -5.413  -1.039  -0.378  1.00  0.00           H  
HETATM   43  H21 UNL     1      -2.468  -2.052  -2.066  1.00  0.00           H  
HETATM   44  H22 UNL     1      -2.935  -2.398   0.398  1.00  0.00           H  
HETATM   45  H23 UNL     1      -0.320  -1.042  -1.628  1.00  0.00           H  
HETATM   46  H24 UNL     1      -1.956  -0.152  -3.300  1.00  0.00           H  
CONECT    1    2   23   24
CONECT    2    3   25   26
CONECT    3    4   11   27
CONECT    4    5   28   29
CONECT    5    6   30   31
CONECT    6    7    8   32
CONECT    7   33   34
CONECT    8    9    9   10
CONECT   10   35
CONECT   11   12
CONECT   12   13   21   36
CONECT   13   14
CONECT   14   15   17   37
CONECT   15   16   38   39
CONECT   16   40
CONECT   17   18   19   41
CONECT   18   42
CONECT   19   20   21   43
CONECT   20   44
CONECT   21   22   45
CONECT   22   46
END

HMDB0242167
     RDKit          3D
5-(Galactosylhydroxy)-L-Lysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    1.4462    0.2654    2.9011 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2068    1.3298    1.9782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    0.9062    0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3272    0.4064   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9385   -0.7925    0.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2041   -1.2420   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2097   -0.2034   -0.1331 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9363   -1.6206   -1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -2.5204   -1.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754   -1.0391   -2.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0002    0.0250    0.4659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0628    0.4898   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527    0.5660    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2721    0.7699   -0.4610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5120    1.3546    0.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2700    2.5851    0.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6450   -0.5627   -1.0597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4699   -1.2058   -0.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685   -1.3626   -1.2067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1346   -2.0182   -0.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -0.4072   -1.4631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3999    0.3256   -2.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7986   -0.5266    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103    0.6495    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585    1.8320    2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0490    2.0484    2.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065    1.8539   -0.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1077    0.2026   -1.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.2420   -0.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2223   -1.6381    0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.6389    1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6039   -2.1226    0.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1503    0.4153    0.7121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1350   -0.6609   -0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -0.0387   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8848    1.5270   -0.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9143    1.4887   -1.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9325    0.6787    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3044    1.4953   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7526    3.3127    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1387   -0.4861   -2.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -1.0394   -0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683   -2.0523   -2.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -2.3975    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3198   -1.0422   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9557   -0.1522   -3.2998 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  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
  3 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
 10 35  1  0
 12 36  1  0
 14 37  1  6
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  6
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Galactosylhydroxylysine	HMDB
Hydroxylysine-galactose	HMDB
beta-1-Galactosyl-O-hydroxylysine	HMDB

Chemical Formula

C₁₂H₂₄N₂O₈

Average Molecular Weight

324.33

Monoisotopic Molecular Weight

324.153265741

IUPAC Name

(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

Traditional Name

(2S)-2,6-diamino-5-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}hexanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O

InChI Identifier

InChI=1S/C12H24N2O8/c13-3-5(1-2-6(14)11(19)20)21-12-10(18)9(17)8(16)7(4-15)22-12/h5-10,12,15-18H,1-4,13-14H2,(H,19,20)/t5?,6-,7+,8-,9-,10+,12?/m0/s1

InChI Key

OWGKYELXGFKIHH-KVUIFDSDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Alpha-amino acid
Alpha-amino acid or derivatives
L-alpha-amino acid
Medium-chain fatty acid
Amino fatty acid
Heterocyclic fatty acid
Hydroxy fatty acid
Sugar acid
Fatty acid
Oxane
Monosaccharide
Secondary alcohol
Amino acid or derivatives
Amino acid
Organoheterocyclic compound
Polyol
Acetal
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Primary amine
Alcohol
Organic oxide
Organopnictogen compound
Primary aliphatic amine
Carbonyl group
Hydrocarbon derivative
Organonitrogen compound
Amine
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Primary alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-3.7	ALOGPS
logP	-6.3	ChemAxon
logS	-0.73	ALOGPS
pKa (Strongest Acidic)	1.85	ChemAxon
pKa (Strongest Basic)	9.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	188.72 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	71.58 m³·mol⁻¹	ChemAxon
Polarizability	31.69 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	171.482	30932474
DeepCCS	[M-H]-	169.586	30932474
DeepCCS	[M-2H]-	202.826	30932474
DeepCCS	[M+Na]+	177.646	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-(Galactosylhydroxy)-L-Lysine	[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O	3494.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine	[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O	3255.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine	[H][C@](N)(CCC([H])(CN)OC1([H])O[C@]([H])(CO)[C@]([H])(O)[C@]([H])(O)[C@@]1([H])O)C(O)=O	2850.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2635.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2852.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3711.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2931.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3018.8	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3463.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2718.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2943.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #11	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3260.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2838.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2962.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3770.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2844.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2955.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3709.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	2948.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3025.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #14	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3405.4	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2910.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3013.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #15	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3379.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C	2937.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C	3034.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #16	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)C(=O)O[Si](C)(C)C	3467.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2905.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3021.7	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #17	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3443.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3155.1	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3117.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3607.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2779.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2910.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #19	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3297.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2679.1	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2849.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(CN)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3661.1	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2859.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2925.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3901.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2856.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2923.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3723.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	2977.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	2987.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #22	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	3463.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2922.1	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2984.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #23	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3415.1	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O	2972.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O	3013.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #24	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O	3505.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2919.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3007.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #25	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3458.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3154.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3112.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3627.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O	2966.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O	2999.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #27	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O	3459.1	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2900.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2998.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #28	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3406.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3143.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3094.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3548.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2721.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2929.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #3	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3266.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3132.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3112.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3609.0	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2720.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2914.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #31	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3197.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32	C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2856.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32	C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2938.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #32	C[Si](C)(C)OC(=O)[C@H](CCC(CN)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3668.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33	C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2851.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33	C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2944.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #33	C[Si](C)(C)OC(=O)[C@@H](N)CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3735.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	2953.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3011.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #34	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3350.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2912.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3001.8	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #35	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3324.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2967.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3019.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #36	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3408.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2929.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3004.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #37	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3387.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3170.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3112.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #38	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3530.4	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	2983.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	2975.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #39	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	3395.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2866.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2956.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3781.1	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2924.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2974.8	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #40	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3346.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41	C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	3161.1	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41	C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	3099.5	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #41	C[Si](C)(C)O[C@H]1C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	3544.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3139.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3082.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3496.0	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2962.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2994.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #43	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3354.4	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2925.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2982.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #44	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3332.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3182.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3086.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #45	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3472.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3157.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3070.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3501.4	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3184.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3107.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3548.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2869.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2946.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3715.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2728.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2947.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #6	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3317.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2856.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2980.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3811.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2858.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2970.7	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3745.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2954.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3035.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3483.0	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2726.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2975.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #1	C[Si](C)(C)NCC(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3076.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2904.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3056.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #10	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3187.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3174.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3130.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	3314.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3156.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3137.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	3362.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	2979.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	3023.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #13	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O	3240.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2919.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3028.7	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #14	C[Si](C)(C)NCC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3195.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3173.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3098.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3342.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3167.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3125.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3371.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3153.9	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3111.7	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3339.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2940.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3035.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #18	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3152.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2910.1	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3031.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #19	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3130.2	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2834.5	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2983.1	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@H](N)C(=O)O[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3649.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3163.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3119.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)N([Si](C)(C)C)[Si](C)(C)C	3271.0	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3191.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3125.4	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3312.3	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO	3168.8	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO	3090.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO	3285.9	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3183.7	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3101.8	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3274.1	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2859.2	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2972.2	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(OC(CN)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3588.6	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2941.3	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3045.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3214.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2916.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3039.9	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #5	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3191.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2936.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3068.6	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3251.8	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2908.6	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3062.0	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #7	C[Si](C)(C)NCC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3229.5	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3183.0	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3139.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(OC(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	3374.7	Standard polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	2932.4	Semi standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3060.3	Standard non polar	33892256
5-(Galactosylhydroxy)-L-Lysine,7TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(CN([Si](C)(C)C)[Si](C)(C)C)OC1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)C(=O)O[Si](C)(C)C	3212.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine GC-MS (Non-derivatized) - 70eV, Positive	splash10-001i-9351000000-2b0869d6c5a1463ed732	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 10V, Positive-QTOF	splash10-0a6u-0149000000-4e725e817251be240bac	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 20V, Positive-QTOF	splash10-004i-2922000000-37a84b130e322e524192	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 40V, Positive-QTOF	splash10-0a4i-6900000000-eef35112d83ae805dfe1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 10V, Negative-QTOF	splash10-0c03-0908000000-de95cb3f8a83dd21606b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 20V, Negative-QTOF	splash10-01ox-2901000000-201eaa6808fc292a80dd	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-(Galactosylhydroxy)-L-Lysine 40V, Negative-QTOF	splash10-0apl-9600000000-b55c13de022050e6e47a	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

65792395

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

66995551

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Kong SW, Hernandez-Ferrer C: Assessment of coverage for endogenous metabolites and exogenous chemical compounds using an untargeted metabolomics platform. Pac Symp Biocomput. 2020;25:587-598. [PubMed:31797630 ]

Showing metabocard for 5-(Galactosylhydroxy)-L-Lysine (HMDB0242167)

MOL for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

3D MOL for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

3D SDF for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

3D-SDF for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

PDB for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

3D PDB for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

SMILES for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

INCHI for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

Structure for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

3D Structure for HMDB0242167 (5-(Galactosylhydroxy)-L-Lysine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra