Hmdb loader

Showing metabocard for Galactosylhydroxylysine (HMDB0000600)

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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 15:47:02 UTC
HMDB IDHMDB0000600
Secondary Accession Numbers
  • HMDB00600
Metabolite Identification
Common NameGalactosylhydroxylysine
DescriptionGalactosylhydroxylysine, also known as hydroxylysine-galactose, belongs to the class of organic compounds known as glycosyl-amino acids. Glycosyl-amino acids are compounds consisting of saccharide linked through a glycosyl linkage (O-, N-, or S-) to an amino acid. Galactosylhydroxylysine has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make galactosylhydroxylysine a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on Galactosylhydroxylysine.
Structure
Data?1582752143
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0000600 (Galactosylhydroxylysine)

Galactosylhydroxylysine.mol
  Mrv1652304202019212D          

 22 22  0  0  0  0            999 V2000
    0.0000    0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.6188    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.4438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.8563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.0938    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.2063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.0313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.8563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.2688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.2688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.0938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.8562    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.0312    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.0312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  1  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  1  9  2  0  0  0  0
  1 10  1  0  0  0  0
  2 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 12 20  1  0  0  0  0
  2 12  1  0  0  0  0
M  END
Download

3D MOL for HMDB0000600 (Galactosylhydroxylysine)

HMDB0000600
     RDKit          3D
Galactosylhydroxylysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    6.5832    0.7644    1.2420 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030    0.9045    0.2037 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3129    0.2731    0.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2521    0.4157   -0.4513 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0156   -0.2341    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8348   -0.1982   -0.8577 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0977   -0.8822   -2.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4347   -1.9162   -2.5045 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0611   -0.4658   -3.0502 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2647   -0.8045   -0.1412 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0374   -2.0973    0.1558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5355   -0.5761   -0.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5712   -1.2688   -0.1783 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -0.6678    0.9259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1695   -1.6298    1.4870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7772   -1.0846    2.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8553    0.6164    0.6137 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2210    0.3982    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692    1.2120   -0.6496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8808    0.6215   -1.7336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7805    0.9339   -0.7448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1189    1.5440    0.3334 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5240   -0.1475    1.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5378    0.9485    0.8386 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3989    1.9772    0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9718    0.3899   -0.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902    0.8441    1.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4092   -0.7750    0.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0752    1.4660   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6229   -0.1004   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7017    0.3620    0.9824 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1934   -1.2590    0.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5826    0.8518   -1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -0.0612   -3.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -2.1378    1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327   -0.8656   -1.8444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3989   -0.4587    1.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6469   -2.5643    1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9252   -1.8772    0.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6241   -1.6619    3.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7204    1.3641    1.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7498    1.0496    1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4056    2.2981   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1732    1.3184   -2.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4126    1.4248   -1.6648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7187    1.7560    1.0748 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
  7  8  2  0
  7  9  1  0
  6 10  1  0
 10 11  1  0
 10 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
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  6
  9 34  1  0
 11 35  1  0
 12 36  1  0
 14 37  1  1
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  1
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END
Download

3D SDF for HMDB0000600 (Galactosylhydroxylysine)

Galactosylhydroxylysine.mol
  Mrv1652304202019212D          

 22 22  0  0  0  0            999 V2000
    0.0000    0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.6188    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.4438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.8563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.0938    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.2063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.0313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.8563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -2.2688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.2688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.0938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.8562    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.0312    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.0312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  1  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  1  9  2  0  0  0  0
  1 10  1  0  0  0  0
  2 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 12 20  1  0  0  0  0
  2 12  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0000600

> <DATABASE_NAME>
hmdb

> <SMILES>
NCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H24N2O8/c13-4-2-1-3-6(12(19)20)14(21)11-10(18)9(17)8(16)7(5-15)22-11/h6-11,15-18,21H,1-5,13H2,(H,19,20)/t6-,7+,8-,9-,10+,11?/m0/s1

> <INCHI_KEY>
RCPOVANIIKXVTB-YPPRVYOWSA-N

> <FORMULA>
C12H24N2O8

> <MOLECULAR_WEIGHT>
324.3276

> <EXACT_MASS>
324.153265754

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.94019637526044

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-3.05

> <JCHEM_LOGP>
-5.336935911754183

> <ALOGPS_LOGS>
-0.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.417213698442694

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9088620171395045

> <JCHEM_PKA_STRONGEST_BASIC>
10.202804242796782

> <JCHEM_POLAR_SURFACE_AREA>
176.94

> <JCHEM_REFRACTIVITY>
72.01079999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.33e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
galactosylhydroxylysine

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0000600 (Galactosylhydroxylysine)

HMDB0000600
     RDKit          3D
Galactosylhydroxylysine
 46 46  0  0  0  0  0  0  0  0999 V2000
    6.5832    0.7644    1.2420 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030    0.9045    0.2037 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3129    0.2731    0.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2521    0.4157   -0.4513 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0156   -0.2341    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8348   -0.1982   -0.8577 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0977   -0.8822   -2.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4347   -1.9162   -2.5045 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0611   -0.4658   -3.0502 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2647   -0.8045   -0.1412 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0374   -2.0973    0.1558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5355   -0.5761   -0.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5712   -1.2688   -0.1783 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -0.6678    0.9259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1695   -1.6298    1.4870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7772   -1.0846    2.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8553    0.6164    0.6137 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2210    0.3982    0.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692    1.2120   -0.6496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8808    0.6215   -1.7336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7805    0.9339   -0.7448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1189    1.5440    0.3334 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5240   -0.1475    1.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5378    0.9485    0.8386 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3989    1.9772    0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9718    0.3899   -0.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902    0.8441    1.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4092   -0.7750    0.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0752    1.4660   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6229   -0.1004   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7017    0.3620    0.9824 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1934   -1.2590    0.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5826    0.8518   -1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -0.0612   -3.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -2.1378    1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327   -0.8656   -1.8444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3989   -0.4587    1.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6469   -2.5643    1.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9252   -1.8772    0.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6241   -1.6619    3.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7204    1.3641    1.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7498    1.0496    1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4056    2.2981   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1732    1.3184   -2.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4126    1.4248   -1.6648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7187    1.7560    1.0748 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
  7  8  2  0
  7  9  1  0
  6 10  1  0
 10 11  1  0
 10 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
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  6
  9 34  1  0
 11 35  1  0
 12 36  1  0
 14 37  1  1
 15 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  1
 20 44  1  0
 21 45  1  6
 22 46  1  0
M  END
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PDB for HMDB0000600 (Galactosylhydroxylysine)

HEADER    PROTEIN                                 20-APR-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Galactosylhydroxylysine.mol                       
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-20         0                                  
HETATM    1  C   UNK     0       0.000   1.155   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       1.334  -1.155   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.334   0.385   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.155   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   2.695   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   3.465   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001   5.005   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.335   5.775   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0      -1.334   0.385   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.000   2.695   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.667  -1.925   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000  -1.925   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -3.465   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -4.235   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334  -4.235   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334  -5.775   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667  -3.465   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.001  -4.235   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.667  -1.925   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.334  -1.155   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.001  -1.155   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.335  -1.925   0.000  0.00  0.00           O+0
CONECT    1    3    9   10                                                  
CONECT    2    3   11   12                                                  
CONECT    3    2    1    4                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    1                                                            
CONECT   10    1                                                            
CONECT   11    2                                                            
CONECT   12   13   20    2                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19   12                                                       
CONECT   21   19   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END
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3D PDB for HMDB0000600 (Galactosylhydroxylysine)

COMPND    HMDB0000600
HETATM    1  N1  UNL     1       6.583   0.764   1.242  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.603   0.905   0.204  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.313   0.273   0.651  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.252   0.416  -0.451  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.016  -0.234   0.078  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.835  -0.198  -0.858  1.00  0.00           C  
HETATM    7  C6  UNL     1       1.098  -0.882  -2.147  1.00  0.00           C  
HETATM    8  O1  UNL     1       0.435  -1.916  -2.505  1.00  0.00           O  
HETATM    9  O2  UNL     1       2.061  -0.466  -3.050  1.00  0.00           O  
HETATM   10  N2  UNL     1      -0.265  -0.805  -0.141  1.00  0.00           N  
HETATM   11  O3  UNL     1      -0.037  -2.097   0.156  1.00  0.00           O  
HETATM   12  C7  UNL     1      -1.535  -0.576  -0.763  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.571  -1.269  -0.178  1.00  0.00           O  
HETATM   14  C8  UNL     1      -3.127  -0.668   0.926  1.00  0.00           C  
HETATM   15  C9  UNL     1      -4.170  -1.630   1.487  1.00  0.00           C  
HETATM   16  O5  UNL     1      -4.777  -1.085   2.615  1.00  0.00           O  
HETATM   17  C10 UNL     1      -3.855   0.616   0.614  1.00  0.00           C  
HETATM   18  O6  UNL     1      -5.221   0.398   0.457  1.00  0.00           O  
HETATM   19  C11 UNL     1      -3.269   1.212  -0.650  1.00  0.00           C  
HETATM   20  O7  UNL     1      -3.881   0.621  -1.734  1.00  0.00           O  
HETATM   21  C12 UNL     1      -1.780   0.934  -0.745  1.00  0.00           C  
HETATM   22  O8  UNL     1      -1.119   1.544   0.333  1.00  0.00           O  
HETATM   23  H1  UNL     1       6.524  -0.147   1.739  1.00  0.00           H  
HETATM   24  H2  UNL     1       7.538   0.949   0.839  1.00  0.00           H  
HETATM   25  H3  UNL     1       5.399   1.977   0.029  1.00  0.00           H  
HETATM   26  H4  UNL     1       5.972   0.390  -0.694  1.00  0.00           H  
HETATM   27  H5  UNL     1       3.890   0.844   1.520  1.00  0.00           H  
HETATM   28  H6  UNL     1       4.409  -0.775   0.940  1.00  0.00           H  
HETATM   29  H7  UNL     1       3.075   1.466  -0.680  1.00  0.00           H  
HETATM   30  H8  UNL     1       3.623  -0.100  -1.378  1.00  0.00           H  
HETATM   31  H9  UNL     1       1.702   0.362   0.982  1.00  0.00           H  
HETATM   32  H10 UNL     1       2.193  -1.259   0.457  1.00  0.00           H  
HETATM   33  H11 UNL     1       0.583   0.852  -1.099  1.00  0.00           H  
HETATM   34  H12 UNL     1       1.749  -0.061  -3.920  1.00  0.00           H  
HETATM   35  H13 UNL     1       0.065  -2.138   1.145  1.00  0.00           H  
HETATM   36  H14 UNL     1      -1.533  -0.866  -1.844  1.00  0.00           H  
HETATM   37  H15 UNL     1      -2.399  -0.459   1.726  1.00  0.00           H  
HETATM   38  H16 UNL     1      -3.647  -2.564   1.753  1.00  0.00           H  
HETATM   39  H17 UNL     1      -4.925  -1.877   0.704  1.00  0.00           H  
HETATM   40  H18 UNL     1      -4.624  -1.662   3.426  1.00  0.00           H  
HETATM   41  H19 UNL     1      -3.720   1.364   1.445  1.00  0.00           H  
HETATM   42  H20 UNL     1      -5.750   1.050   1.010  1.00  0.00           H  
HETATM   43  H21 UNL     1      -3.406   2.298  -0.679  1.00  0.00           H  
HETATM   44  H22 UNL     1      -4.173   1.318  -2.371  1.00  0.00           H  
HETATM   45  H23 UNL     1      -1.413   1.425  -1.665  1.00  0.00           H  
HETATM   46  H24 UNL     1      -1.719   1.756   1.075  1.00  0.00           H  
CONECT    1    2   23   24
CONECT    2    3   25   26
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7   10   33
CONECT    7    8    8    9
CONECT    9   34
CONECT   10   11   12
CONECT   11   35
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
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SMILES for HMDB0000600 (Galactosylhydroxylysine)

NCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O
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INCHI for HMDB0000600 (Galactosylhydroxylysine)

InChI=1S/C12H24N2O8/c13-4-2-1-3-6(12(19)20)14(21)11-10(18)9(17)8(16)7(5-15)22-11/h6-11,15-18,21H,1-5,13H2,(H,19,20)/t6-,7+,8-,9-,10+,11?/m0/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
5-(beta-D-Galactopyranosyloxy)-L-lysineHMDB
5-(beta-delta-Galactopyranosyloxy)-L-lysineHMDB
5-O-beta-D-Galactopyranosylhydroxy-L-lysineHMDB
5-O-beta-delta-Galactopyranosylhydroxy-L-lysineHMDB
beta-1-Galactosyl-O-hydroxylysineHMDB
Galactopyranosylhydroxy-L-lysineHMDB
Galactosyl-delta-hydroxylysineHMDB
Hydroxylysine-galactoseHMDB
L-5-(beta-D-Galactopyranosyloxy)-lysineHMDB
L-5-(beta-delta-Galactopyranosyloxy)-lysineHMDB
O-beta-D-Galactopyranosylhydroxy-L-lysineHMDB
O-beta-delta-Galactopyranosylhydroxy-L-lysineHMDB
Procollagen (5-galactosyloxy)-L-lysineHMDB
(2S)-6-Amino-2-{n-hydroxy[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}hexanoateHMDB
Chemical FormulaC12H24N2O8
Average Molecular Weight324.3276
Monoisotopic Molecular Weight324.153265754
IUPAC Name(2S)-6-amino-2-{N-hydroxy[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino}hexanoic acid
Traditional Namegalactosylhydroxylysine
CAS Registry Number32448-36-5
SMILES
NCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O
InChI Identifier
InChI=1S/C12H24N2O8/c13-4-2-1-3-6(12(19)20)14(21)11-10(18)9(17)8(16)7(5-15)22-11/h6-11,15-18,21H,1-5,13H2,(H,19,20)/t6-,7+,8-,9-,10+,11?/m0/s1
InChI KeyRCPOVANIIKXVTB-YPPRVYOWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as glycosyl-amino acids. Glycosyl-amino acids are compounds consisting of saccharide linked through a glycosyl linkage (O-, N-, or S-) to an amino acid.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentGlycosyl-amino acids
Alternative Parents
Substituents
  • Glycosyl-amino-acid
  • Hexose monosaccharide
  • Glycosyl compound
  • N-glycosyl compound
  • N-hydroxyl-alpha-amino acid
  • Alpha-amino acid or derivatives
  • Medium-chain fatty acid
  • Amino fatty acid
  • Heterocyclic fatty acid
  • Hydroxy fatty acid
  • Monosaccharide
  • Oxane
  • Fatty acyl
  • Fatty acid
  • Secondary alcohol
  • Amino acid
  • Organoheterocyclic compound
  • Polyol
  • Carboxylic acid
  • Oxacycle
  • N-organohydroxylamine
  • Monocarboxylic acid or derivatives
  • Primary amine
  • Primary aliphatic amine
  • Alcohol
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organic oxide
  • Organopnictogen compound
  • Carbonyl group
  • Organic oxygen compound
  • Primary alcohol
  • Organic nitrogen compound
  • Amine
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
Role
Industrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point257.0 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility63.3 g/LALOGPS
logP-3ALOGPS
logP-5.3ChemAxon
logS-0.71ALOGPS
pKa (Strongest Acidic)3.91ChemAxon
pKa (Strongest Basic)10.2ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area176.94 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity72.01 m³·mol⁻¹ChemAxon
Polarizability31.94 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+175.77431661259
DarkChem[M-H]-174.80731661259
AllCCS[M+H]+171.92532859911
AllCCS[M-H]-173.8332859911
DeepCCS[M+H]+178.51530932474
DeepCCS[M+H]+175.73730932474
DeepCCS[M-H]-176.15730932474
DeepCCS[M-H]-173.37930932474
DeepCCS[M-2H]-210.06530932474
DeepCCS[M+Na]+186.22730932474
DeepCCS[M-2H]-206.30630932474
DeepCCS[M+Na]+181.8330932474
AllCCS[M+H]+171.932859911
AllCCS[M+H-H2O]+169.132859911
AllCCS[M+NH4]+174.532859911
AllCCS[M+Na]+175.332859911
AllCCS[M-H]-173.832859911
AllCCS[M+Na-2H]-173.732859911
AllCCS[M+HCOO]-173.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
GalactosylhydroxylysineNCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O3145.5Standard polar33892256
GalactosylhydroxylysineNCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O2890.9Standard non polar33892256
GalactosylhydroxylysineNCCCC[C@H](N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(O)=O2777.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Galactosylhydroxylysine,1TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O2706.0Semi standard non polar33892256
Galactosylhydroxylysine,1TMS,isomer #2C[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@H]1O2689.1Semi standard non polar33892256
Galactosylhydroxylysine,1TMS,isomer #3C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@@H]1O2678.3Semi standard non polar33892256
Galactosylhydroxylysine,1TMS,isomer #4C[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN)C(=O)O)O[C@H](CO)[C@H](O)[C@@H]1O2706.8Semi standard non polar33892256
Galactosylhydroxylysine,1TMS,isomer #5C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O2673.0Semi standard non polar33892256
Galactosylhydroxylysine,1TMS,isomer #6C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O2816.9Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O2653.9Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2651.5Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #11C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@@H]1O[Si](C)(C)C2695.8Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #12C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2797.5Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #13C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2640.8Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #14C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2824.8Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #15C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O2775.8Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #16C[Si](C)(C)N(CCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C2953.6Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O2718.1Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O2689.1Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C2691.7Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #5C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O2825.9Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2640.6Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #7C[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN)C(=O)O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O2689.2Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #8C[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C2677.0Semi standard non polar33892256
Galactosylhydroxylysine,2TMS,isomer #9C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2796.6Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O2635.1Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #10C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2781.7Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O2931.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2635.7Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #13C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2641.8Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #14C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2727.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #15C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(N(O)[C@@H](CCCCN)C(=O)O)O[C@@H]1CO2690.6Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #16C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2797.8Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #17C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2782.1Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #18C[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@H]1O2903.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #19C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2655.4Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O2651.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #20C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2739.3Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #21C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2792.4Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #22C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@@H]1O2921.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #23C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2729.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #24C[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[C@H](CO)[C@H](O)[C@@H]1O2940.1Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O2901.2Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C2629.6Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #4C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O2727.9Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2698.6Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #6C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2682.5Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #7C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2790.5Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2671.5Semi standard non polar33892256
Galactosylhydroxylysine,3TMS,isomer #9C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2797.8Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2667.9Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #10C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2789.6Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O2933.6Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #12C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2768.9Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #13C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O2921.6Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #14C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C2908.7Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2656.3Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #16C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2735.1Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #17C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2752.4Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #18C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2895.3Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #19C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2778.5Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2656.2Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #20C[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O2929.1Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #21C[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C2900.6Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #22C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2742.5Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2912.0Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #24C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@@H]1O[Si](C)(C)C2930.1Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2917.8Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #3C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2735.8Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2658.1Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #5C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2751.8Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #6C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2729.5Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #7C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O2892.5Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #8C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2683.0Semi standard non polar33892256
Galactosylhydroxylysine,4TMS,isomer #9C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2784.2Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2666.1Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #10C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2950.6Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #11C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2924.0Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #12C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2738.6Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #13C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2914.5Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #14C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2944.6Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #15C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[C@@H]1CO2937.7Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #16C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2938.1Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #2C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2747.7Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #3C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2751.3Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O2938.8Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #5C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2741.0Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #6C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O2939.1Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #7C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C2920.7Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #8C[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[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)C2775.2Semi standard non polar33892256
Galactosylhydroxylysine,5TMS,isomer #9C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2949.0Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #1C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[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)C2749.8Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #1C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[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)C2841.0Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #1C[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C)N(O)C1O[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)C3139.6Standard polar33892256
Galactosylhydroxylysine,6TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2962.2Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O2910.6Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #2C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O3307.9Standard polar33892256
Galactosylhydroxylysine,6TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2955.6Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C2930.5Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #3C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C3356.8Standard polar33892256
Galactosylhydroxylysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2937.0Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2928.3Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #4C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3302.3Standard polar33892256
Galactosylhydroxylysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2953.3Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2880.5Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #5C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3309.2Standard polar33892256
Galactosylhydroxylysine,6TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2941.5Semi standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2895.7Standard non polar33892256
Galactosylhydroxylysine,6TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3247.2Standard polar33892256
Galactosylhydroxylysine,7TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2959.4Semi standard non polar33892256
Galactosylhydroxylysine,7TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2948.3Standard non polar33892256
Galactosylhydroxylysine,7TMS,isomer #1C[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3120.7Standard polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O2969.3Semi standard non polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@H]1O2958.3Semi standard non polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@@H]1O2955.1Semi standard non polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN)C(=O)O)O[C@H](CO)[C@H](O)[C@@H]1O2971.9Semi standard non polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O2941.7Semi standard non polar33892256
Galactosylhydroxylysine,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O3078.7Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O3144.0Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3155.1Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3179.6Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3290.5Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3178.4Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3301.9Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O3269.7Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)N(CCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C3395.2Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O3191.1Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3167.6Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3156.7Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O3280.2Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3158.3Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN)C(=O)O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3174.7Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3166.8Semi standard non polar33892256
Galactosylhydroxylysine,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3285.9Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O3378.7Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3482.9Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O3606.6Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3337.4Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3344.3Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3472.6Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(N(O)[C@@H](CCCCN)C(=O)O)O[C@@H]1CO3358.1Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3485.8Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3481.3Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@H]1O3606.5Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3349.0Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3368.3Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3486.1Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3482.4Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@@H]1O3606.9Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3492.3Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[C@H](CO)[C@H](O)[C@@H]1O3617.5Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O3582.9Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3338.6Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O3463.3Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3364.4Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3365.5Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3504.0Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3359.4Semi standard non polar33892256
Galactosylhydroxylysine,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3494.3Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3523.8Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3676.3Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O3827.7Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3673.1Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3807.0Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3798.9Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3499.6Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3647.9Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3646.9Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3790.2Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3661.0Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3516.2Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@H]1C(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3796.3Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3790.5Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3640.8Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3788.2Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3791.7Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3795.9Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3662.2Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3524.4Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3677.6Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3642.8Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O3788.5Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3550.5Semi standard non polar33892256
Galactosylhydroxylysine,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3676.1Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3712.6Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4003.0Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3991.1Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #12CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3796.4Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3954.0Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3963.3Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[C@@H]1CO3969.0Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3949.5Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3826.0Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3815.7Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O3989.3Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3823.9Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3982.6Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3963.5Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #8CC(C)(C)[Si](C)(C)NCCCC[C@@H](C(=O)O)N(O)C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3846.7Semi standard non polar33892256
Galactosylhydroxylysine,5TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1OC(N(O)[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3994.4Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0pbl-9331000000-55f681ebb00dbb5b63ad2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (5 TMS) - 70eV, Positivesplash10-01c0-3922126000-4608c9d1673267935e9e2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Galactosylhydroxylysine GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Galactosylhydroxylysine CE-QTOF-MS system (Agilent 7100 CE + 6550 QTOF) 20V, Positive-QTOFsplash10-03fs-0900000000-b277425c7b2baf2e1ce02019-03-07HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 10V, Positive-QTOFsplash10-0a6r-0319000000-e7265dc7d65b37c433702016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 20V, Positive-QTOFsplash10-0c04-5934000000-12517f6dca52703813c32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 40V, Positive-QTOFsplash10-03dl-7910000000-7645fde658d9539753152016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 10V, Negative-QTOFsplash10-0udi-0692000000-ce838deeac1950cd53172016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 20V, Negative-QTOFsplash10-0nu9-0961000000-0121d6fb23dab2a0d4482016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 40V, Negative-QTOFsplash10-0abc-6910000000-955acf234208503cf7362016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 10V, Positive-QTOFsplash10-004i-0009000000-feb8033fade4ec36b1632021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 20V, Positive-QTOFsplash10-00kb-1900000000-9887ff59cd8b2608215e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 40V, Positive-QTOFsplash10-0a59-9500000000-2e6b65bbf11b1b8a689f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 10V, Negative-QTOFsplash10-00di-0309000000-6517fbb0bf566b43f2d02021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 20V, Negative-QTOFsplash10-00di-5769000000-812154ea65e633cab3a02021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Galactosylhydroxylysine 40V, Negative-QTOFsplash10-00kf-4900000000-d6a34ed61253e7556f1d2021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm (predicted from logP)
Biospecimen Locations
  • Blood
  • Urine
Tissue Locations
  • Platelet
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.061 +/- 0.008 uMAdult (>18 years old)BothNormal details
UrineDetected and Quantified1.35 (0.45-2.3) umol/mmol creatinineAdult (>18 years old)MaleNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.11 +/- 0.01 uMAdult (>18 years old)BothPaget's disease (osteitis deformans) details
UrineDetected and Quantified1.03 +/- 0.48 umol/mmol creatinineAdult (>18 years old)FemaleOsteoporosis details
UrineDetected and Quantified1.35 +/- 0.82 umol/mmol creatinineAdult (>18 years old)FemaleOsteoporosis details
Associated Disorders and Diseases
Disease References
Paget's disease
  1. Al-Dehaimi AW, Blumsohn A, Eastell R: Serum galactosyl hydroxylysine as a biochemical marker of bone resorption. Clin Chem. 1999 May;45(5):676-81. [PubMed:10222355 ]
Osteoporosis
  1. Lo Cascio V, Bertoldo F, Gambaro G, Gasperi E, Furlan F, Colapietro F, Lo Cascio C, Campagnola M: Urinary galactosyl-hydroxylysine in postmenopausal osteoporotic women: A potential marker of bone fragility. J Bone Miner Res. 1999 Aug;14(8):1420-4. [PubMed:10457275 ]
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB112162
KNApSAcK IDNot Available
Chemspider ID17215976
KEGG Compound IDC05547
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID5576
PubChem Compound22833535
PDB IDNot Available
ChEBI ID165859
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00000196
Good Scents IDNot Available
References
Synthesis ReferenceAdamczyk, Maciej; Reddy, Rajarathnam E.; Rege, Sushil D. Synthesis of galactosylhydroxylysine and its analogs. Synthetic Communications (2000), 30(18), 3281-3290.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Kelleher PC: Urinary excretion of hydroxyproline, hydroxylysine and hydroxylysine glycosides by patients with Paget's disease of bone and carcinoma with metastases in bone. Clin Chim Acta. 1979 Mar 15;92(3):373-9. [PubMed:436278 ]
  2. Schroder CH, Monnens LA, van Lith-Zanders HM, Trijbels JM, Veerkamp JH: The urinary excretion of total hydroxylysine and its glycosides in normal persons, and in patients suffering from Alport's syndrome--contribution of the peptide-bound fraction. Nephron. 1987;47(4):253-7. [PubMed:3696326 ]
  3. Schroder CH, Langeveld JP, van Raay-Selten BH, Trijbels FJ, de Graaf R, Veerkamp JH, Monnens LA: Urinary excretion of hydroxylysine and its glycosides in normal persons of different ages--influence of maturation. Int J Pediatr Nephrol. 1985 Oct-Dec;6(4):239-44. [PubMed:2419268 ]
  4. Schroder CH, Monnens LA, van Lith-Zanders HM, Trijbels JM, Veerkamp JH, Langeveld JP: Urinary excretion of hydroxylysine and its glycosides in Alport's syndrome and several other glomerulopathies. Nephron. 1986;44(2):103-7. [PubMed:3774073 ]
  5. Grazioli V, Alfano M, Stenico A, Casari E: Urinary output of hydroxylysine glycosides and pyridinium cross-links in detecting rat bone collagen turnover rate. FEBS Lett. 1996 Jun 17;388(2-3):134-8. [PubMed:8690072 ]
  6. Marabini R, Sirtori P, Chionna R, Barzizza L, Rubinacci A: Galactosylhydroxylysine and pyridinium cross links in monitoring the bone response to hormone replacement therapy. J Endocrinol Invest. 1996 Mar;19(3):154-8. [PubMed:8743280 ]
  7. Leigh SD, Ju HS, Lundgard R, Daniloff GY, Liu V: Development of an immunoassay for urinary galactosylhydroxylysine. J Immunol Methods. 1998 Nov 1;220(1-2):169-78. [PubMed:9839938 ]
  8. Sirtori P, Sosio C, Polo RM, Tenni R, Rubinacci A: A comparative study on biochemical markers of bone collagen breakdown in post-menopausal women. Pharmacol Res. 1997 Sep;36(3):229-35. [PubMed:9367668 ]
  9. LoCascio V, Braga V, Bertoldo F, Bettica P, Pasini AF, Stefani L, Moro L: Effect of bisphosphonate therapy and parathyroidectomy on the urinary excretion of galactosylhydroxylysine in primary hyperparathyroidism. Clin Endocrinol (Oxf). 1994 Jul;41(1):47-51. [PubMed:8050131 ]
  10. Al-Dehaimi AW, Blumsohn A, Eastell R: Serum galactosyl hydroxylysine as a biochemical marker of bone resorption. Clin Chem. 1999 May;45(5):676-81. [PubMed:10222355 ]
  11. Casetta B, Romanello M, Moro L: A rapid and simple method for quantitation of urinary hydroxylysyl glycosides, indicators of collagen turnover, using liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom. 2000;14(23):2238-41. [PubMed:11114034 ]
  12. Plebani M, Bernardi D, Meneghetti MF, Ujka F, Zaninotto M: Biological variability in assessing the clinical value of biochemical markers of bone turnover. Clin Chim Acta. 2000 Sep;299(1-2):77-86. [PubMed:10900294 ]
  13. (). Moro, L., Romanello, M. Galactosylhydroxylysine and bone metabolism: an updated review. Cells and Materials (1997), 7(4), 329-332. .
  14. (). Kakimoto, Y., Akazawa, Shigenori. Isolation and identification of NG,NG- and NG,N'G-dimethylarginine, N -mono-, di-, and trimethyllysine, and glucosylgalactosyl- and galactosyl- -hydroxylysine from human urine. Journal of Biological Chemistry (1970), 245(21), 5751-8. .