Hmdb loader

Showing metabocard for Hyaluronan biosynthesis, precursor 1 (HMDB0060071)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-09 20:52:28 UTC
Update Date2022-03-07 03:17:38 UTC
HMDB IDHMDB0060071
Secondary Accession Numbers
  • HMDB60071
Metabolite Identification
Common NameHyaluronan biosynthesis, precursor 1
DescriptionHyaluronan biosynthesis, precursor 1, also known as b-D-4-deoxy-delta(4)-glca-(1->3)-b-D-glcnac, belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group. Hyaluronan biosynthesis, precursor 1 is a moderately basic compound (based on its pKa). These are carbohydrate derivatives containing a hexose moeity in which the oxygen atom is replaced by an n-acyl group.
Structure
Data?1563866012
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)


  Mrv0541 05091313522D          

 26 27  0  0  0  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  4  0  0  0
  5  2  1  0  0  0  0
  6  2  2  0  0  0  0
  7  3  1  1  0  0  0
  9  5  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15  4  2  0  0  0  0
  8 15  1  6  0  0  0
 16  3  1  0  0  0  0
 17  4  1  0  0  0  0
  5 18  1  1  0  0  0
  9 19  1  6  0  0  0
 10 20  1  6  0  0  0
 21 12  2  0  0  0  0
 22 12  1  0  0  0  0
 13 23  1  1  0  0  0
 24  7  1  0  0  0  0
 24 13  1  0  0  0  0
 25  6  1  0  0  0  0
 25 14  1  0  0  0  0
 11 26  1  1  0  0  0
 14 26  1  1  0  0  0
M  END
Download

3D MOL for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

HMDB0060071
     RDKit          3D
Hyaluronan biosynthesis, precursor 1
 47 48  0  0  0  0  0  0  0  0999 V2000
    3.3820    2.2500   -1.7763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1668    2.6557   -1.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8067    3.9946   -1.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4324    1.8562   -0.3577 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7084    0.4273   -0.2474 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9240    0.1892    0.5686 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7658   -0.6854   -0.1260 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -0.2958    1.8247 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7593   -1.1533    2.0777 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2355   -2.3395    2.8936 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7450   -1.8822    4.0990 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.6129    0.8229 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0677   -2.5395    1.0677 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4792   -0.3042    0.2530 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4064   -0.5655   -0.7828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6897   -0.1525   -0.5448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6176   -1.2246   -0.4940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9683   -0.8604   -0.3625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9750   -1.8540   -0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1845   -1.5379    0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6484   -3.1919    0.1925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3640    0.3885   -0.5460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4418    1.4961   -0.8995 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0087    2.4524   -1.7018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2160    0.8407   -1.5488 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3143    1.8132   -1.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4318    2.8568   -2.7077 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3598    1.1932   -2.1019 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3102    2.4814   -1.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3563    4.3415   -1.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8569    0.0734   -1.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4897    1.1545    0.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6392   -0.7976    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9852   -0.6431    2.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702   -2.9531    2.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3518   -2.9847    3.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3410   -2.5644    4.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8438   -1.9912    0.1297 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1423   -3.2878    0.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0180    0.1943    1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7363    0.3241    0.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9327   -3.4856    0.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4195    0.6668   -0.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0595    1.9078    0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2834    2.9673   -2.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6248    0.2849   -2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4542    2.0975   -2.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 18 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  5  1  0
 25 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  5 31  1  6
  6 32  1  1
  7 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  6
 13 39  1  0
 14 40  1  1
 16 41  1  1
 21 42  1  0
 22 43  1  0
 23 44  1  1
 24 45  1  0
 25 46  1  6
 26 47  1  0
M  END
Download

3D SDF for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)


  Mrv0541 05091313522D          

 26 27  0  0  0  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  4  0  0  0
  5  2  1  0  0  0  0
  6  2  2  0  0  0  0
  7  3  1  1  0  0  0
  9  5  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15  4  2  0  0  0  0
  8 15  1  6  0  0  0
 16  3  1  0  0  0  0
 17  4  1  0  0  0  0
  5 18  1  1  0  0  0
  9 19  1  6  0  0  0
 10 20  1  6  0  0  0
 21 12  2  0  0  0  0
 22 12  1  0  0  0  0
 13 23  1  1  0  0  0
 24  7  1  0  0  0  0
 24 13  1  0  0  0  0
 25  6  1  0  0  0  0
 25 14  1  0  0  0  0
 11 26  1  1  0  0  0
 14 26  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0060071

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H21NO11/c1-4(17)15-8-11(10(20)7(3-16)24-13(8)23)26-14-9(19)5(18)2-6(25-14)12(21)22/h2,5,7-11,13-14,16,18-20,23H,3H2,1H3,(H,15,17)(H,21,22)/t5-,7+,8+,9+,10+,11+,13+,14-/m0/s1

> <INCHI_KEY>
DLGJWSVWTWEWBJ-UCFDOFRFSA-N

> <FORMULA>
C14H21NO11

> <MOLECULAR_WEIGHT>
379.3166

> <EXACT_MASS>
379.111460519

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
34.31922868815841

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S)-2-{[(2R,3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}-3,4-dihydroxy-3,4-dihydro-2H-pyran-6-carboxylic acid

> <ALOGPS_LOGP>
-2.59

> <JCHEM_LOGP>
-3.2142602790539083

> <ALOGPS_LOGS>
-0.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.2476387195661065

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.112823890808677

> <JCHEM_PKA_STRONGEST_BASIC>
1.2367084032184077

> <JCHEM_POLAR_SURFACE_AREA>
198.72999999999996

> <JCHEM_REFRACTIVITY>
80.1881

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.11e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5R,6R)-6-{[(2R,3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}-4,5-dihydroxy-5,6-dihydro-4H-pyran-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

HMDB0060071
     RDKit          3D
Hyaluronan biosynthesis, precursor 1
 47 48  0  0  0  0  0  0  0  0999 V2000
    3.3820    2.2500   -1.7763 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1668    2.6557   -1.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8067    3.9946   -1.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4324    1.8562   -0.3577 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7084    0.4273   -0.2474 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9240    0.1892    0.5686 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7658   -0.6854   -0.1260 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7645   -0.2958    1.8247 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7593   -1.1533    2.0777 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2355   -2.3395    2.8936 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7450   -1.8822    4.0990 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.6129    0.8229 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0677   -2.5395    1.0677 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4792   -0.3042    0.2530 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4064   -0.5655   -0.7828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6897   -0.1525   -0.5448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6176   -1.2246   -0.4940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9683   -0.8604   -0.3625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9750   -1.8540   -0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1845   -1.5379    0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6484   -3.1919    0.1925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3640    0.3885   -0.5460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4418    1.4961   -0.8995 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0087    2.4524   -1.7018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2160    0.8407   -1.5488 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3143    1.8132   -1.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4318    2.8568   -2.7077 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3598    1.1932   -2.1019 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3102    2.4814   -1.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3563    4.3415   -1.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8569    0.0734   -1.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4897    1.1545    0.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6392   -0.7976    0.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9852   -0.6431    2.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702   -2.9531    2.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3518   -2.9847    3.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3410   -2.5644    4.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8438   -1.9912    0.1297 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1423   -3.2878    0.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0180    0.1943    1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7363    0.3241    0.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9327   -3.4856    0.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4195    0.6668   -0.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0595    1.9078    0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2834    2.9673   -2.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6248    0.2849   -2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4542    2.0975   -2.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 18 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  5  1  0
 25 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  5 31  1  6
  6 32  1  1
  7 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  6
 13 39  1  0
 14 40  1  1
 16 41  1  1
 21 42  1  0
 22 43  1  0
 23 44  1  1
 24 45  1  0
 25 46  1  6
 26 47  1  0
M  END
Download

PDB for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

HEADER    PROTEIN                                 09-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-MAY-13         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -1.334  -6.930   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
CONECT    1    4                                                            
CONECT    2    5    6                                                       
CONECT    3    7   16                                                       
CONECT    4    1   15   17                                                  
CONECT    5    2    9   18                                                  
CONECT    6    2   12   25                                                  
CONECT    7    3   10   24                                                  
CONECT    8   11   13   15                                                  
CONECT    9    5   14   19                                                  
CONECT   10    7   11   20                                                  
CONECT   11    8   10   26                                                  
CONECT   12    6   21   22                                                  
CONECT   13    8   23   24                                                  
CONECT   14    9   25   26                                                  
CONECT   15    4    8                                                       
CONECT   16    3                                                            
CONECT   17    4                                                            
CONECT   18    5                                                            
CONECT   19    9                                                            
CONECT   20   10                                                            
CONECT   21   12                                                            
CONECT   22   12                                                            
CONECT   23   13                                                            
CONECT   24    7   13                                                       
CONECT   25    6   14                                                       
CONECT   26   11   14                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END
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3D PDB for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

COMPND    HMDB0060071
HETATM    1  C1  UNL     1       3.382   2.250  -1.776  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.167   2.656  -1.028  1.00  0.00           C  
HETATM    3  O1  UNL     1       1.807   3.995  -1.062  1.00  0.00           O  
HETATM    4  N1  UNL     1       1.432   1.856  -0.358  1.00  0.00           N  
HETATM    5  C3  UNL     1       1.708   0.427  -0.247  1.00  0.00           C  
HETATM    6  C4  UNL     1       2.924   0.189   0.569  1.00  0.00           C  
HETATM    7  O2  UNL     1       3.766  -0.685  -0.126  1.00  0.00           O  
HETATM    8  O3  UNL     1       2.764  -0.296   1.825  1.00  0.00           O  
HETATM    9  C5  UNL     1       1.759  -1.153   2.078  1.00  0.00           C  
HETATM   10  C6  UNL     1       2.236  -2.340   2.894  1.00  0.00           C  
HETATM   11  O4  UNL     1       2.745  -1.882   4.099  1.00  0.00           O  
HETATM   12  C7  UNL     1       1.048  -1.613   0.823  1.00  0.00           C  
HETATM   13  O5  UNL     1       0.068  -2.539   1.068  1.00  0.00           O  
HETATM   14  C8  UNL     1       0.479  -0.304   0.253  1.00  0.00           C  
HETATM   15  O6  UNL     1      -0.406  -0.566  -0.783  1.00  0.00           O  
HETATM   16  C9  UNL     1      -1.690  -0.153  -0.545  1.00  0.00           C  
HETATM   17  O7  UNL     1      -2.618  -1.225  -0.494  1.00  0.00           O  
HETATM   18  C10 UNL     1      -3.968  -0.860  -0.362  1.00  0.00           C  
HETATM   19  C11 UNL     1      -4.975  -1.854  -0.019  1.00  0.00           C  
HETATM   20  O8  UNL     1      -6.184  -1.538   0.101  1.00  0.00           O  
HETATM   21  O9  UNL     1      -4.648  -3.192   0.193  1.00  0.00           O  
HETATM   22  C12 UNL     1      -4.364   0.388  -0.546  1.00  0.00           C  
HETATM   23  C13 UNL     1      -3.442   1.496  -0.899  1.00  0.00           C  
HETATM   24  O10 UNL     1      -4.009   2.452  -1.702  1.00  0.00           O  
HETATM   25  C14 UNL     1      -2.216   0.841  -1.549  1.00  0.00           C  
HETATM   26  O11 UNL     1      -1.314   1.813  -1.899  1.00  0.00           O  
HETATM   27  H1  UNL     1       3.432   2.857  -2.708  1.00  0.00           H  
HETATM   28  H2  UNL     1       3.360   1.193  -2.102  1.00  0.00           H  
HETATM   29  H3  UNL     1       4.310   2.481  -1.212  1.00  0.00           H  
HETATM   30  H4  UNL     1       1.356   4.342  -1.913  1.00  0.00           H  
HETATM   31  H5  UNL     1       1.857   0.073  -1.297  1.00  0.00           H  
HETATM   32  H6  UNL     1       3.490   1.155   0.635  1.00  0.00           H  
HETATM   33  H7  UNL     1       4.639  -0.798   0.344  1.00  0.00           H  
HETATM   34  H8  UNL     1       0.985  -0.643   2.705  1.00  0.00           H  
HETATM   35  H9  UNL     1       2.970  -2.953   2.326  1.00  0.00           H  
HETATM   36  H10 UNL     1       1.352  -2.985   3.084  1.00  0.00           H  
HETATM   37  H11 UNL     1       3.341  -2.564   4.486  1.00  0.00           H  
HETATM   38  H12 UNL     1       1.844  -1.991   0.130  1.00  0.00           H  
HETATM   39  H13 UNL     1       0.142  -3.288   0.415  1.00  0.00           H  
HETATM   40  H14 UNL     1      -0.018   0.194   1.089  1.00  0.00           H  
HETATM   41  H15 UNL     1      -1.736   0.324   0.477  1.00  0.00           H  
HETATM   42  H16 UNL     1      -3.933  -3.486   0.839  1.00  0.00           H  
HETATM   43  H17 UNL     1      -5.420   0.667  -0.442  1.00  0.00           H  
HETATM   44  H18 UNL     1      -3.059   1.908   0.071  1.00  0.00           H  
HETATM   45  H19 UNL     1      -3.283   2.967  -2.146  1.00  0.00           H  
HETATM   46  H20 UNL     1      -2.625   0.285  -2.429  1.00  0.00           H  
HETATM   47  H21 UNL     1      -1.454   2.097  -2.858  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    4    4
CONECT    3   30
CONECT    4    5
CONECT    5    6   14   31
CONECT    6    7    8   32
CONECT    7   33
CONECT    8    9
CONECT    9   10   12   34
CONECT   10   11   35   36
CONECT   11   37
CONECT   12   13   14   38
CONECT   13   39
CONECT   14   15   40
CONECT   15   16
CONECT   16   17   25   41
CONECT   17   18
CONECT   18   19   22   22
CONECT   19   20   20   21
CONECT   21   42
CONECT   22   23   43
CONECT   23   24   25   44
CONECT   24   45
CONECT   25   26   46
CONECT   26   47
END
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SMILES for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O
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INCHI for HMDB0060071 (Hyaluronan biosynthesis, precursor 1)

InChI=1S/C14H21NO11/c1-4(17)15-8-11(10(20)7(3-16)24-13(8)23)26-14-9(19)5(18)2-6(25-14)12(21)22/h2,5,7-11,13-14,16,18-20,23H,3H2,1H3,(H,15,17)(H,21,22)/t5-,7+,8+,9+,10+,11+,13+,14-/m0/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
2-(Acetylamino)-2-deoxy-3-O-(4-deoxy-alpha-L-threo-hex-4-enopyranuronosyl)-beta-D-glucopyranoseChEBI
3-(4-Deoxy-alpha-L-threo-hex-4-enopyranosyluronic acid)-2-acetamido-2-deoxy-D-glucoseChEBI
3-(4-Deoxy-beta-D-gluc-4-enuronosyl)-N-acetyl-D-glucosamineChEBI
beta-D-4-Deoxy-Delta(4)-glca-(1->3)-beta-D-glcnacChEBI
2-(Acetylamino)-2-deoxy-3-O-(4-deoxy-a-L-threo-hex-4-enopyranuronosyl)-b-D-glucopyranoseGenerator
2-(Acetylamino)-2-deoxy-3-O-(4-deoxy-α-L-threo-hex-4-enopyranuronosyl)-β-D-glucopyranoseGenerator
3-(4-Deoxy-a-L-threo-hex-4-enopyranosyluronate)-2-acetamido-2-deoxy-D-glucoseGenerator
3-(4-Deoxy-a-L-threo-hex-4-enopyranosyluronic acid)-2-acetamido-2-deoxy-D-glucoseGenerator
3-(4-Deoxy-alpha-L-threo-hex-4-enopyranosyluronate)-2-acetamido-2-deoxy-D-glucoseGenerator
3-(4-Deoxy-α-L-threo-hex-4-enopyranosyluronate)-2-acetamido-2-deoxy-D-glucoseGenerator
3-(4-Deoxy-α-L-threo-hex-4-enopyranosyluronic acid)-2-acetamido-2-deoxy-D-glucoseGenerator
3-(4-Deoxy-b-D-gluc-4-enuronosyl)-N-acetyl-D-glucosamineGenerator
3-(4-Deoxy-β-D-gluc-4-enuronosyl)-N-acetyl-D-glucosamineGenerator
b-D-4-Deoxy-delta(4)-glca-(1->3)-b-D-glcnacGenerator
Β-D-4-deoxy-δ(4)-glca-(1->3)-β-D-glcnacGenerator
3-(4-Deoxy-b-D-gluc-4-enosyluronate)-N-acetyl-D-glucosamineHMDB
3-(4-Deoxy-b-D-gluc-4-enosyluronic acid)-N-acetyl-D-glucosamineHMDB
3-(4-Deoxy-beta-D-gluc-4-enosyluronate)-N-acetyl-D-glucosamineHMDB
3-(4-Deoxy-β-D-gluc-4-enosyluronate)-N-acetyl-D-glucosamineHMDB
3-(4-Deoxy-β-D-gluc-4-enosyluronic acid)-N-acetyl-D-glucosamineHMDB
b-D-4-Deoxy-δ(4)-glca-(1->3)-b-D-glcnacHMDB
Chemical FormulaC14H21NO11
Average Molecular Weight379.3166
Monoisotopic Molecular Weight379.111460519
IUPAC Name(2R,3R,4S)-2-{[(2R,3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}-3,4-dihydroxy-3,4-dihydro-2H-pyran-6-carboxylic acid
Traditional Name(4S,5R,6R)-6-{[(2R,3R,4R,5S,6R)-2,5-dihydroxy-3-[(1-hydroxyethylidene)amino]-6-(hydroxymethyl)oxan-4-yl]oxy}-4,5-dihydroxy-5,6-dihydro-4H-pyran-2-carboxylic acid
CAS Registry NumberNot Available
SMILES
CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O
InChI Identifier
InChI=1S/C14H21NO11/c1-4(17)15-8-11(10(20)7(3-16)24-13(8)23)26-14-9(19)5(18)2-6(25-14)12(21)22/h2,5,7-11,13-14,16,18-20,23H,3H2,1H3,(H,15,17)(H,21,22)/t5-,7+,8+,9+,10+,11+,13+,14-/m0/s1
InChI KeyDLGJWSVWTWEWBJ-UCFDOFRFSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentAcylaminosugars
Alternative Parents
Substituents
  • Acylaminosugar
  • N-acyl-alpha-hexosamine
  • Disaccharide
  • Oxane
  • Acetamide
  • Carboxamide group
  • Hemiacetal
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Acetal
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Oxacycle
  • Organoheterocyclic compound
  • Organic oxide
  • Alcohol
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Carbonyl group
  • Organonitrogen compound
  • Organopnictogen compound
  • Primary alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
DispositionNot Available
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility51.1 g/LALOGPS
logP-2.6ALOGPS
logP-3.2ChemAxon
logS-0.87ALOGPS
pKa (Strongest Acidic)3.11ChemAxon
pKa (Strongest Basic)1.24ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area198.73 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity80.19 m³·mol⁻¹ChemAxon
Polarizability34.32 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
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]+183.94431661259
DarkChem[M-H]-175.21331661259
DeepCCS[M+H]+175.99530932474
DeepCCS[M-H]-173.92630932474
DeepCCS[M-2H]-207.16630932474
DeepCCS[M+Na]+181.89430932474
AllCCS[M+H]+184.632859911
AllCCS[M+H-H2O]+181.932859911
AllCCS[M+NH4]+187.032859911
AllCCS[M+Na]+187.832859911
AllCCS[M-H]-182.432859911
AllCCS[M+Na-2H]-182.132859911
AllCCS[M+HCOO]-182.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Hyaluronan biosynthesis, precursor 1CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O4677.7Standard polar33892256
Hyaluronan biosynthesis, precursor 1CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O3098.6Standard non polar33892256
Hyaluronan biosynthesis, precursor 1CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(=C[C@H](O)[C@H]1O)C(O)=O3167.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #1CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2970.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #2CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2921.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #3CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2919.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #4CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2920.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #5CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2954.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #6CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2926.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TMS,isomer #7CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2872.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2948.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #10CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2937.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #11CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2892.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #12CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2888.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #13CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2828.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #14CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2933.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #15CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2893.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #16CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2800.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #17CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2928.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #18CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2885.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #19CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2858.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #2CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2946.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #20CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2942.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #21CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2821.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #3CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2928.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #4CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2907.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #5CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2993.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #6CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2968.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #7CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2885.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #8CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2877.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TMS,isomer #9CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2816.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2872.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #10CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2781.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #11CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2906.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #12CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2879.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #13CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2815.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #14CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2819.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #15CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2933.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #16CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O2833.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #17CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2789.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #18CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2900.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #19CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2870.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2850.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #20CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2758.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #21CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2889.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #22CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2846.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #23CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2808.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #24CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2798.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #25CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2916.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #26CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2797.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #27CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2902.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #28CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2876.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #29CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2824.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2806.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #30CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2815.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #31CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2913.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #32CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2796.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #33CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2783.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #34CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2896.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #35CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2819.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2933.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2901.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #6CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2872.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #7CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2820.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #8CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2932.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TMS,isomer #9CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2909.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2780.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #10CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2906.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #11CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2758.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #12CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2865.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #13CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2850.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #14CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2786.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #15CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2797.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #16CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2897.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #17CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2768.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #18CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2761.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #19CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2883.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2756.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #20CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2809.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #21CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O2772.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #22CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O2866.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #23CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C2840.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #24CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2819.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #25CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2825.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #26CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2902.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #27CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2802.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #28CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2797.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #29CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2881.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2862.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #30CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2847.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #31CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2825.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #32CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2821.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #33CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2901.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #34CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2849.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #35CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2827.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2844.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2727.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #6CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2856.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #7CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2818.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #8CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2783.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TMS,isomer #9CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2784.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C2705.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #10CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2802.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #11CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2766.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #12CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2751.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #13CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2836.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #14CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2794.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #15CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2771.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #16CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O2812.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #17CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C2793.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #18CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2873.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #19CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2849.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2807.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #20CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2825.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #21CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2846.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2770.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2767.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2760.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #6CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2848.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #7CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2747.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #8CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2721.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,5TMS,isomer #9CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2836.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C2769.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2737.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2818.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2793.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2765.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #6CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2778.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,6TMS,isomer #7CC(O)=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2833.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,7TMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C)=C[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C2801.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #1CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3197.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #2CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3145.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #3CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3151.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #4CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3133.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #5CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3171.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #6CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3155.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,1TBDMS,isomer #7CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3122.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3343.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #10CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3326.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #11CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3316.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #12CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3300.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #13CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3282.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #14CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3325.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #15CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3319.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #16CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3250.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #17CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3316.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #18CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3304.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #19CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3297.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #2CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3347.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #20CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3334.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #21CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3289.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #3CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3324.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #4CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3337.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #5CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3393.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #6CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3392.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #7CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3288.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #8CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3282.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,2TBDMS,isomer #9CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3275.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3493.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #10CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3439.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #11CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3529.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #12CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3523.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #13CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3494.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #14CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3491.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #15CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3549.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #16CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O3465.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #17CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3436.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #18CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3504.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #19CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3491.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3474.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #20CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3415.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #21CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3499.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #22CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3481.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #23CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3455.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #24CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3446.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #25CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3518.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #26CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3439.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #27CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3514.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #28CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3502.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #29CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3468.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3465.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #30CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3459.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #31CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3522.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #32CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3439.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #33CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3426.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #34CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3510.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #35CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(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)C3470.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3551.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3541.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #6CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3494.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #7CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3473.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #8CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3551.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,3TBDMS,isomer #9CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3545.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #1CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3626.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #10CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3729.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #11CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3584.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #12CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3700.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #13CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3676.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #14CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3634.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #15CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3621.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #16CC(=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3718.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #17CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3615.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #18CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3595.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #19CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3707.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #2CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3589.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #20CC(=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(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)C)O[Si](C)(C)C(C)(C)C3663.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #21CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O3583.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #22CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3675.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #23CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3657.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #24CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3612.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #25CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3607.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #26CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3689.6Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #27CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3591.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #28CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3584.7Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #29CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3682.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #3CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3699.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #30CC(O)=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(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)C3638.0Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #31CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3625.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #32CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3619.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #33CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3700.4Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #34CC(O)=N[C@H]1[C@H](O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(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)C3646.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #35CC(O)=N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(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)C3630.3Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #4CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3675.5Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #5CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C3562.2Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #6CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3690.8Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #7CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1OC(C(=O)O)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3659.1Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #8CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C3646.9Semi standard non polar33892256
Hyaluronan biosynthesis, precursor 1,4TBDMS,isomer #9CC(=N[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1OC(C(=O)O[Si](C)(C)C(C)(C)C)=C[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3624.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Hyaluronan biosynthesis, precursor 1 GC-MS (Non-derivatized) - 70eV, Positivesplash10-0229-9245000000-f93299417c022ace0dd22017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Hyaluronan biosynthesis, precursor 1 GC-MS (4 TMS) - 70eV, Positivesplash10-0udl-9100125000-0b1ed86790addfe386f52017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Hyaluronan biosynthesis, precursor 1 GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Hyaluronan biosynthesis, precursor 1 GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 10V, Positive-QTOFsplash10-0h90-0169000000-a40df014ee5a187c18682017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 20V, Positive-QTOFsplash10-0uk9-1493000000-6b4cc1076d17a105fc352017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 40V, Positive-QTOFsplash10-0umi-7890000000-44ef953438b8d3392b852017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 10V, Negative-QTOFsplash10-005i-4339000000-99892fc0e7705786280f2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 20V, Negative-QTOFsplash10-0fk9-7597000000-091f8f5113b376ae985e2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hyaluronan biosynthesis, precursor 1 40V, Negative-QTOFsplash10-0pb9-9500000000-ff39213001c0f079dcc62017-10-06Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDC04794
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound440484
PDB IDNot Available
ChEBI ID16126
Food Biomarker OntologyNot Available
VMH IDHA_PRE1
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Thiele I, Swainston N, Fleming RM, Hoppe A, Sahoo S, Aurich MK, Haraldsdottir H, Mo ML, Rolfsson O, Stobbe MD, Thorleifsson SG, Agren R, Bolling C, Bordel S, Chavali AK, Dobson P, Dunn WB, Endler L, Hala D, Hucka M, Hull D, Jameson D, Jamshidi N, Jonsson JJ, Juty N, Keating S, Nookaew I, Le Novere N, Malys N, Mazein A, Papin JA, Price ND, Selkov E Sr, Sigurdsson MI, Simeonidis E, Sonnenschein N, Smallbone K, Sorokin A, van Beek JH, Weichart D, Goryanin I, Nielsen J, Westerhoff HV, Kell DB, Mendes P, Palsson BO: A community-driven global reconstruction of human metabolism. Nat Biotechnol. 2013 May;31(5):419-25. doi: 10.1038/nbt.2488. Epub 2013 Mar 3. [PubMed:23455439 ]