Hmdb loader

Showing metabocard for O-Ureidohomoserine (HMDB0012271)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-04-06 16:22:06 UTC
Update Date2023-02-21 17:17:47 UTC
HMDB IDHMDB0012271
Secondary Accession Numbers
  • HMDB12271
Metabolite Identification
Common NameO-Ureidohomoserine
DescriptionO-Ureidohomoserine is involved in the canavanine biosynthesis pathway. It can be generated from the enzymatic reduction of canavaninosuccinate or enzymatic oxidation of L-canaline. The canavanine biosynthesis pathway is analogous to the animal Krebs-Henseleit ornithine-urea cycle. Feeding experiments demonstrated the existence of enzyme activities of canaline-dependent ornithine carbamyltransferase, ureidohomoserine-dependent argininosuccinate synthetase, and canavaninosuccinate-dependent argininosuccinate lyase in Canavalia lineate. The canaline-dependent ornithine carbamyltransferase has been purified subsequently. The synthesis of ureidohomoserine is probably the rate-limiting step. Ureidohomoserine interacted with canaline or canavanine to affect synergistically L. minor growth by enhancing individual canavanine or canaline toxicity and increasing the additive growth reduction caused by canavanine plus canaline. The ornithineurea cycle amino acids effectively counteracted both the additive and synergistic growth-inhibiting properties of the canaline-urea cycle compounds.(PMID: 16659513 ).
Structure
Data?1676999867
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0012271 (O-Ureidohomoserine)


  Mrv0541 02241203542D          

 12 11  0  0  0  0            999 V2000
   10.9335  -11.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7584  -11.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5210  -11.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9335  -12.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4083   -9.6989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6961  -11.8418    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2332   -9.6989    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.9958  -10.4128    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.5210  -13.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7584  -12.5564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9958   -8.9844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1709  -10.4128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  3  1  0  0  0  0
  1  2  1  0  0  0  0
  2 12  1  0  0  0  0
  3  6  1  0  0  0  0
  3  4  1  0  0  0  0
  4  9  1  0  0  0  0
  4 10  2  0  0  0  0
  5  8  1  0  0  0  0
  5  7  2  0  0  0  0
  5 11  1  0  0  0  0
  8 12  1  0  0  0  0
M  END
Download

3D MOL for HMDB0012271 (O-Ureidohomoserine)

HMDB0012271
     RDKit          3D
O-Ureidohomoserine
 23 22  0  0  0  0  0  0  0  0999 V2000
   -4.2521   -1.0175    0.2489 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4788   -0.0480   -0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8134    1.2331    0.3122 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3048   -0.3157   -0.8126 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1237   -0.6305   -0.2621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4774    0.5407    0.1256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8701    0.2440    0.7576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7603   -0.4891   -0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9384    0.3484   -1.3980 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0652   -0.7791    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1408   -1.4956    1.4388 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2329   -0.2508   -0.1194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1148   -2.0100    0.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9553    1.9968   -0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4063   -0.2533   -1.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1141    1.0240    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3280    1.2462   -0.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -0.3105    1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3843    1.2015    0.9781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062   -1.4403   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3891    0.0570   -2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9597    0.4588   -1.5842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5543    0.6900    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 10 12  1  0
  1 13  1  0
  3 14  1  0
  4 15  1  0
  6 16  1  0
  6 17  1  0
  7 18  1  0
  7 19  1  0
  8 20  1  0
  9 21  1  0
  9 22  1  0
 12 23  1  0
M  END
Download

3D SDF for HMDB0012271 (O-Ureidohomoserine)


  Mrv0541 02241203542D          

 12 11  0  0  0  0            999 V2000
   10.9335  -11.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7584  -11.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5210  -11.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9335  -12.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4083   -9.6989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6961  -11.8418    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2332   -9.6989    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.9958  -10.4128    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.5210  -13.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7584  -12.5564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9958   -8.9844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1709  -10.4128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  3  1  0  0  0  0
  1  2  1  0  0  0  0
  2 12  1  0  0  0  0
  3  6  1  0  0  0  0
  3  4  1  0  0  0  0
  4  9  1  0  0  0  0
  4 10  2  0  0  0  0
  5  8  1  0  0  0  0
  5  7  2  0  0  0  0
  5 11  1  0  0  0  0
  8 12  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0012271

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(CCONC(O)=N)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C5H11N3O4/c6-3(4(9)10)1-2-12-8-5(7)11/h3H,1-2,6H2,(H,9,10)(H3,7,8,11)

> <INCHI_KEY>
SFYVZOSIAIZWQU-UHFFFAOYSA-N

> <FORMULA>
C5H11N3O4

> <MOLECULAR_WEIGHT>
177.1585

> <EXACT_MASS>
177.074955855

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
16.475540380308544

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-4-{[(C-hydroxycarbonimidoyl)amino]oxy}butanoic acid

> <ALOGPS_LOGP>
-3.45

> <JCHEM_LOGP>
-3.400054945574937

> <ALOGPS_LOGS>
-1.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.091726168353333

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9168404315483976

> <JCHEM_PKA_STRONGEST_BASIC>
9.58656515468146

> <JCHEM_POLAR_SURFACE_AREA>
128.66000000000003

> <JCHEM_REFRACTIVITY>
59.58610000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.49e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-4-[(C-hydroxycarbonimidoylamino)oxy]butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0012271 (O-Ureidohomoserine)

HMDB0012271
     RDKit          3D
O-Ureidohomoserine
 23 22  0  0  0  0  0  0  0  0999 V2000
   -4.2521   -1.0175    0.2489 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4788   -0.0480   -0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8134    1.2331    0.3122 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3048   -0.3157   -0.8126 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1237   -0.6305   -0.2621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4774    0.5407    0.1256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8701    0.2440    0.7576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7603   -0.4891   -0.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9384    0.3484   -1.3980 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0652   -0.7791    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1408   -1.4956    1.4388 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2329   -0.2508   -0.1194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1148   -2.0100    0.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9553    1.9968   -0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4063   -0.2533   -1.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1141    1.0240    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3280    1.2462   -0.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -0.3105    1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3843    1.2015    0.9781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062   -1.4403   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3891    0.0570   -2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9597    0.4588   -1.5842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5543    0.6900    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 10 12  1  0
  1 13  1  0
  3 14  1  0
  4 15  1  0
  6 16  1  0
  6 17  1  0
  7 18  1  0
  7 19  1  0
  8 20  1  0
  9 21  1  0
  9 22  1  0
 12 23  1  0
M  END
Download

PDB for HMDB0012271 (O-Ureidohomoserine)

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      20.409 -20.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.949 -20.771   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.639 -22.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.409 -23.439   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      25.029 -18.105   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      18.099 -22.105   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      26.569 -18.105   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0      24.259 -19.437   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0      19.639 -24.772   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      21.949 -23.439   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      24.259 -16.771   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      22.719 -19.437   0.000  0.00  0.00           O+0
CONECT    1    3    2                                                       
CONECT    2    1   12                                                       
CONECT    3    1    6    4                                                  
CONECT    4    3    9   10                                                  
CONECT    5    8    7   11                                                  
CONECT    6    3                                                            
CONECT    7    5                                                            
CONECT    8    5   12                                                       
CONECT    9    4                                                            
CONECT   10    4                                                            
CONECT   11    5                                                            
CONECT   12    2    8                                                       
MASTER        0    0    0    0    0    0    0    0   12    0   22    0
END
Download

3D PDB for HMDB0012271 (O-Ureidohomoserine)

COMPND    HMDB0012271
HETATM    1  N1  UNL     1      -4.252  -1.018   0.249  1.00  0.00           N  
HETATM    2  C1  UNL     1      -3.479  -0.048  -0.073  1.00  0.00           C  
HETATM    3  O1  UNL     1      -3.813   1.233   0.312  1.00  0.00           O  
HETATM    4  N2  UNL     1      -2.305  -0.316  -0.813  1.00  0.00           N  
HETATM    5  O2  UNL     1      -1.124  -0.630  -0.262  1.00  0.00           O  
HETATM    6  C2  UNL     1      -0.477   0.541   0.126  1.00  0.00           C  
HETATM    7  C3  UNL     1       0.870   0.244   0.758  1.00  0.00           C  
HETATM    8  C4  UNL     1       1.760  -0.489  -0.245  1.00  0.00           C  
HETATM    9  N3  UNL     1       1.938   0.348  -1.398  1.00  0.00           N  
HETATM   10  C5  UNL     1       3.065  -0.779   0.410  1.00  0.00           C  
HETATM   11  O3  UNL     1       3.141  -1.496   1.439  1.00  0.00           O  
HETATM   12  O4  UNL     1       4.233  -0.251  -0.119  1.00  0.00           O  
HETATM   13  H1  UNL     1      -4.115  -2.010   0.023  1.00  0.00           H  
HETATM   14  H2  UNL     1      -3.955   1.997  -0.329  1.00  0.00           H  
HETATM   15  H3  UNL     1      -2.406  -0.253  -1.870  1.00  0.00           H  
HETATM   16  H4  UNL     1      -1.114   1.024   0.893  1.00  0.00           H  
HETATM   17  H5  UNL     1      -0.328   1.246  -0.716  1.00  0.00           H  
HETATM   18  H6  UNL     1       0.767  -0.310   1.706  1.00  0.00           H  
HETATM   19  H7  UNL     1       1.384   1.202   0.978  1.00  0.00           H  
HETATM   20  H8  UNL     1       1.306  -1.440  -0.555  1.00  0.00           H  
HETATM   21  H9  UNL     1       1.389   0.057  -2.218  1.00  0.00           H  
HETATM   22  H10 UNL     1       2.960   0.459  -1.584  1.00  0.00           H  
HETATM   23  H11 UNL     1       4.554   0.690   0.146  1.00  0.00           H  
CONECT    1    2    2   13
CONECT    2    3    4
CONECT    3   14
CONECT    4    5   15
CONECT    5    6
CONECT    6    7   16   17
CONECT    7    8   18   19
CONECT    8    9   10   20
CONECT    9   21   22
CONECT   10   11   11   12
CONECT   12   23
END
Download

SMILES for HMDB0012271 (O-Ureidohomoserine)

NC(CCONC(O)=N)C(O)=O
Download

INCHI for HMDB0012271 (O-Ureidohomoserine)

InChI=1S/C5H11N3O4/c6-3(4(9)10)1-2-12-8-5(7)11/h3H,1-2,6H2,(H,9,10)(H3,7,8,11)
Download
View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
alpha-amino-gamma-Ureidooxybutyric acidHMDB
O-((Aminocarbonyl)amino)-L-homoserineHMDB
O-ureido-L-HomoserineHMDB
2-Amino-4-{[(C-hydroxycarbonimidoyl)amino]oxy}butanoateGenerator
O-UreidohomoserineMeSH
Chemical FormulaC5H11N3O4
Average Molecular Weight177.1585
Monoisotopic Molecular Weight177.074955855
IUPAC Name2-amino-4-{[(C-hydroxycarbonimidoyl)amino]oxy}butanoic acid
Traditional Name2-amino-4-[(C-hydroxycarbonimidoylamino)oxy]butanoic acid
CAS Registry Number51767-67-0
SMILES
NC(CCONC(O)=N)C(O)=O
InChI Identifier
InChI=1S/C5H11N3O4/c6-3(4(9)10)1-2-12-8-5(7)11/h3H,1-2,6H2,(H,9,10)(H3,7,8,11)
InChI KeySFYVZOSIAIZWQU-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentAlpha amino acids
Alternative Parents
Substituents
  • Alpha-amino acid
  • Fatty acid
  • Carbonic acid derivative
  • Amino acid
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organopnictogen compound
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Primary aliphatic amine
  • Carbonyl group
  • Amine
  • Hydrocarbon derivative
  • Organic oxide
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Route of exposureSource
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
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 Solubility2.49 g/LALOGPS
logP-3.4ALOGPS
logP-3.4ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)1.92ChemAxon
pKa (Strongest Basic)9.59ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area128.66 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity59.59 m³·mol⁻¹ChemAxon
Polarizability16.48 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+138.52831661259
DarkChem[M-H]-133.07731661259
DeepCCS[M+H]+131.72630932474
DeepCCS[M-H]-128.07230932474
DeepCCS[M-2H]-165.53630932474
DeepCCS[M+Na]+140.67630932474
AllCCS[M+H]+139.432859911
AllCCS[M+H-H2O]+135.732859911
AllCCS[M+NH4]+143.032859911
AllCCS[M+Na]+144.032859911
AllCCS[M-H]-134.932859911
AllCCS[M+Na-2H]-136.532859911
AllCCS[M+HCOO]-138.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
O-UreidohomoserineNC(CCONC(O)=N)C(O)=O2950.9Standard polar33892256
O-UreidohomoserineNC(CCONC(O)=N)C(O)=O1971.9Standard non polar33892256
O-UreidohomoserineNC(CCONC(O)=N)C(O)=O2106.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
O-Ureidohomoserine,1TMS,isomer #1C[Si](C)(C)OC(=N)NOCCC(N)C(=O)O1941.7Semi standard non polar33892256
O-Ureidohomoserine,1TMS,isomer #2C[Si](C)(C)OC(=O)C(N)CCONC(=N)O1936.2Semi standard non polar33892256
O-Ureidohomoserine,1TMS,isomer #3C[Si](C)(C)NC(CCONC(=N)O)C(=O)O2040.4Semi standard non polar33892256
O-Ureidohomoserine,1TMS,isomer #4C[Si](C)(C)N(OCCC(N)C(=O)O)C(=N)O2016.0Semi standard non polar33892256
O-Ureidohomoserine,1TMS,isomer #5C[Si](C)(C)N=C(O)NOCCC(N)C(=O)O1948.6Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #1C[Si](C)(C)OC(=N)NOCCC(N)C(=O)O[Si](C)(C)C1962.5Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #10C[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C)C(=O)O2032.0Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O)[Si](C)(C)C2016.9Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #2C[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C)C(=O)O2039.4Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #3C[Si](C)(C)N=C(NOCCC(N)C(=O)O)O[Si](C)(C)C1915.9Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #4C[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O)[Si](C)(C)C1992.1Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #5C[Si](C)(C)NC(CCONC(=N)O)C(=O)O[Si](C)(C)C2030.6Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #6C[Si](C)(C)OC(=O)C(N)CCON(C(=N)O)[Si](C)(C)C1988.4Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #7C[Si](C)(C)N=C(O)NOCCC(N)C(=O)O[Si](C)(C)C1942.8Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #8C[Si](C)(C)N(C(CCONC(=N)O)C(=O)O)[Si](C)(C)C2180.4Semi standard non polar33892256
O-Ureidohomoserine,2TMS,isomer #9C[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C)C(=O)O2101.6Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #1C[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2043.8Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #1C[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C)C(=O)O[Si](C)(C)C1886.7Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #1C[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3009.0Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #10C[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C2010.9Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #10C[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C1803.6Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #10C[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C2796.4Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1998.2Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1880.9Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C2964.2Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #12C[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=N)O2209.1Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #12C[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=N)O1968.0Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #12C[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=N)O2880.5Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #13C[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C2168.3Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #13C[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C1901.5Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #13C[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C2960.3Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #14C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C2071.1Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #14C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C1892.9Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #14C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C2862.6Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #2C[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C1917.0Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #2C[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C1764.5Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #2C[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3183.1Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #3C[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1967.6Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #3C[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1942.4Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #3C[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C3158.6Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #4C[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C2181.7Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #4C[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C1950.9Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #4C[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3145.7Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #5C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O2050.3Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #5C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O1953.6Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #5C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O2992.6Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #6C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O)O[Si](C)(C)C1984.7Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #6C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O)O[Si](C)(C)C1782.7Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #6C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O)O[Si](C)(C)C3073.5Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C1944.1Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C1902.2Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C3175.0Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #8C[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C)[Si](C)(C)C2138.6Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #8C[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C)[Si](C)(C)C1865.7Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #8C[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C)[Si](C)(C)C2779.7Standard polar33892256
O-Ureidohomoserine,3TMS,isomer #9C[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C2036.5Semi standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #9C[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C1916.5Standard non polar33892256
O-Ureidohomoserine,3TMS,isomer #9C[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C2686.6Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #1C[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2169.3Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #1C[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1985.5Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #1C[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2786.2Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #10C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2065.5Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #10C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C1905.4Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #10C[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2544.3Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2195.2Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2000.8Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #11C[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2707.5Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #2C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2031.1Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #2C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2009.2Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #2C[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2590.3Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #3C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C1982.0Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #3C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C1805.3Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #3C[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C2696.6Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1942.2Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C1925.4Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C2746.5Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #5C[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2150.0Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #5C[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C1879.1Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #5C[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2840.8Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #6C[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2183.6Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #6C[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2095.7Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #6C[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2787.8Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C2014.7Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C1959.8Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #7C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O)[Si](C)(C)C2549.7Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2180.8Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2049.8Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2557.6Standard polar33892256
O-Ureidohomoserine,4TMS,isomer #9C[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2134.5Semi standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #9C[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1886.5Standard non polar33892256
O-Ureidohomoserine,4TMS,isomer #9C[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2653.2Standard polar33892256
O-Ureidohomoserine,5TMS,isomer #1C[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2157.2Semi standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #1C[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C1898.6Standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #1C[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2564.8Standard polar33892256
O-Ureidohomoserine,5TMS,isomer #2C[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2198.8Semi standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #2C[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2117.5Standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #2C[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2471.1Standard polar33892256
O-Ureidohomoserine,5TMS,isomer #3C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2008.4Semi standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #3C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C1978.7Standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #3C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2222.2Standard polar33892256
O-Ureidohomoserine,5TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2193.5Semi standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2066.5Standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #4C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2391.7Standard polar33892256
O-Ureidohomoserine,5TMS,isomer #5C[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2223.4Semi standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #5C[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2006.2Standard non polar33892256
O-Ureidohomoserine,5TMS,isomer #5C[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2482.2Standard polar33892256
O-Ureidohomoserine,6TMS,isomer #1C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2243.1Semi standard non polar33892256
O-Ureidohomoserine,6TMS,isomer #1C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2081.7Standard non polar33892256
O-Ureidohomoserine,6TMS,isomer #1C[Si](C)(C)N=C(O[Si](C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2176.8Standard polar33892256
O-Ureidohomoserine,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=N)NOCCC(N)C(=O)O2205.5Semi standard non polar33892256
O-Ureidohomoserine,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)C(N)CCONC(=N)O2198.8Semi standard non polar33892256
O-Ureidohomoserine,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(CCONC(=N)O)C(=O)O2292.5Semi standard non polar33892256
O-Ureidohomoserine,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(OCCC(N)C(=O)O)C(=N)O2248.4Semi standard non polar33892256
O-Ureidohomoserine,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N)C(=O)O2221.4Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=N)NOCCC(N)C(=O)O[Si](C)(C)C(C)(C)C2431.4Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O2514.0Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O)[Si](C)(C)C(C)(C)C2478.2Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O2536.6Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(NOCCC(N)C(=O)O)O[Si](C)(C)C(C)(C)C2401.3Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O)[Si](C)(C)C(C)(C)C2450.4Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(CCONC(=N)O)C(=O)O[Si](C)(C)C(C)(C)C2509.0Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)C(N)CCON(C(=N)O)[Si](C)(C)C(C)(C)C2432.8Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N)C(=O)O[Si](C)(C)C(C)(C)C2439.8Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)N(C(CCONC(=N)O)C(=O)O)[Si](C)(C)C(C)(C)C2601.8Semi standard non polar33892256
O-Ureidohomoserine,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)C(=O)O2563.9Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2717.4Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2433.4Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCONC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3015.0Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2659.5Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2297.5Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2885.7Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2633.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2395.7Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3037.3Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=N)O2835.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=N)O2514.8Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=N)O2940.2Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2811.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2403.0Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2990.5Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2729.3Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2399.3Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2960.6Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2582.9Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2272.6Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)N=C(NOCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3118.0Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2618.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2511.7Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3105.8Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2829.1Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2467.5Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3107.4Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2723.2Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2505.9Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3019.7Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)C2673.0Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)C2263.0Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)C3023.6Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C(C)(C)C2609.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C(C)(C)C2434.0Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O)[Si](C)(C)C(C)(C)C3087.6Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2768.6Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2438.9Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCONC(=N)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2862.9Standard polar33892256
O-Ureidohomoserine,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2691.8Semi standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2498.5Standard non polar33892256
O-Ureidohomoserine,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2834.6Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3025.9Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2665.3Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=N)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2960.9Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2870.3Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2563.9Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2858.3Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3028.9Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2652.7Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2949.1Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2879.8Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2698.3Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCON(C(=N)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2865.5Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2840.1Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2433.8Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(NOCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2879.5Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2792.3Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2603.3Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2921.8Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2998.9Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2508.8Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2956.6Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3031.9Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2735.7Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2954.8Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2855.5Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2609.7Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C2812.2Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3009.2Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2770.3Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCON(C(=N)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2841.5Standard polar33892256
O-Ureidohomoserine,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2981.6Semi standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2568.1Standard non polar33892256
O-Ureidohomoserine,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C(O)NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2895.2Standard polar33892256
O-Ureidohomoserine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3197.1Semi standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2699.4Standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(NOCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2859.5Standard polar33892256
O-Ureidohomoserine,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3235.0Semi standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2936.1Standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=N)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2838.6Standard polar33892256
O-Ureidohomoserine,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3015.5Semi standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2773.2Standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2717.9Standard polar33892256
O-Ureidohomoserine,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3206.5Semi standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2843.5Standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2770.2Standard polar33892256
O-Ureidohomoserine,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3191.0Semi standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2822.2Standard non polar33892256
O-Ureidohomoserine,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)N=C(O)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2853.4Standard polar33892256
O-Ureidohomoserine,6TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3422.9Semi standard non polar33892256
O-Ureidohomoserine,6TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3023.2Standard non polar33892256
O-Ureidohomoserine,6TBDMS,isomer #1CC(C)(C)[Si](C)(C)N=C(O[Si](C)(C)C(C)(C)C)N(OCCC(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2759.7Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - O-Ureidohomoserine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9200000000-09018d8ebfc327cf6e322017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - O-Ureidohomoserine GC-MS (2 TMS) - 70eV, Positivesplash10-00di-9361000000-031b96a404c08397958f2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - O-Ureidohomoserine 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 - O-Ureidohomoserine 10V, Positive-QTOFsplash10-0m1i-2900000000-caf76614b9c4ed5917262017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 20V, Positive-QTOFsplash10-0a4i-9600000000-f9253e2fdf27205b30cf2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 40V, Positive-QTOFsplash10-0a4i-9000000000-3de115bbc46c6215bcfd2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 10V, Negative-QTOFsplash10-0059-2900000000-66b67d20b11e1030a2b22017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 20V, Negative-QTOFsplash10-0006-9300000000-41b0080d162a10f336412017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 40V, Negative-QTOFsplash10-0006-9000000000-7ceaac484332cd2488e12017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 10V, Negative-QTOFsplash10-054o-9100000000-a91ad1e4a8cccb4304872021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 20V, Negative-QTOFsplash10-052f-9200000000-2abda3789392ed608dfe2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 40V, Negative-QTOFsplash10-0006-9000000000-16d7c771f9c36fd947292021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 10V, Positive-QTOFsplash10-02di-1900000000-7a6d25877ba4e3db2ab92021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 20V, Positive-QTOFsplash10-0a4i-9300000000-e468a2309943903fa5962021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - O-Ureidohomoserine 40V, Positive-QTOFsplash10-0a4i-9000000000-cf7b4dbdb040a515988c2021-09-24Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-03FELIX 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 IDFDB028907
KNApSAcK IDNot Available
Chemspider ID19993690
KEGG Compound IDNot Available
BioCyc IDO-UREIDOHOMOSERINE
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound21126175
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Rosenthal GA, Gulati DK, Sabharwal PS: Additive and Synergistic Growth-inhibiting Properties of the Canaline-Urea Cycle Amino Acids. Plant Physiol. 1976 Apr;57(4):493-6. [PubMed:16659513 ]