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Showing metabocard for (S)-2-Amino-4-methylpentanamide (HMDB0247199)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 00:12:39 UTC
Update Date2021-09-26 22:56:44 UTC
HMDB IDHMDB0247199
Secondary Accession NumbersNone
Metabolite Identification
Common Name(S)-2-Amino-4-methylpentanamide
Description(S)-2-Amino-4-methylpentanamide, also known as leucinamide, belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review a significant number of articles have been published on (S)-2-Amino-4-methylpentanamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). (s)-2-amino-4-methylpentanamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (S)-2-Amino-4-methylpentanamide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)


  Mrv1652309112102122D          

  9  8  0  0  0  0            999 V2000
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.9520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  5  9  1  0  0  0  0
M  END
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3D MOL for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

HMDB0247199
     RDKit          3D
(S)-2-Amino-4-methylpentanamide
 23 22  0  0  0  0  0  0  0  0999 V2000
   -2.3343    1.2326   -0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654    0.2567    0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9808   -1.1009    0.1972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667    0.3628   -0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9983   -0.5453    0.0329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3063   -0.2635    1.3876 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2342   -0.3017   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4516    0.1369   -0.1842 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2228   -0.4818   -2.0260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7775    2.2035   -0.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2120    1.4362    0.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6439    0.8552   -1.4100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    0.6013    1.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -0.9821    0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5549   -1.7904    0.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601   -1.5399   -0.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2973    1.4089   -0.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2625    0.1379   -1.5815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7611   -1.6174   -0.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7293    0.4303    1.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6831   -1.0230    1.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8476    1.0919   -0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9601   -0.5081    0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  2  0
  1 10  1  0
  1 11  1  0
  1 12  1  0
  2 13  1  0
  3 14  1  0
  3 15  1  0
  3 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  0
  6 20  1  0
  6 21  1  0
  8 22  1  0
  8 23  1  0
M  END
Download

3D SDF for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)


  Mrv1652309112102122D          

  9  8  0  0  0  0            999 V2000
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.9520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  5  9  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247199

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CC(N)C(N)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H14N2O/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H2,8,9)

> <INCHI_KEY>
FORGMRSGVSYZQR-UHFFFAOYSA-N

> <FORMULA>
C6H14N2O

> <MOLECULAR_WEIGHT>
130.191

> <EXACT_MASS>
130.110613079

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
14.693902407946979

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-4-methylpentanamide

> <ALOGPS_LOGP>
-0.51

> <JCHEM_LOGP>
-0.13154377199999986

> <ALOGPS_LOGS>
-0.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.691843256777897

> <JCHEM_PKA_STRONGEST_BASIC>
8.439612115646714

> <JCHEM_POLAR_SURFACE_AREA>
69.11

> <JCHEM_REFRACTIVITY>
35.9931

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.78e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-4-methylpentanamide

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

HMDB0247199
     RDKit          3D
(S)-2-Amino-4-methylpentanamide
 23 22  0  0  0  0  0  0  0  0999 V2000
   -2.3343    1.2326   -0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654    0.2567    0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9808   -1.1009    0.1972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667    0.3628   -0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9983   -0.5453    0.0329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3063   -0.2635    1.3876 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2342   -0.3017   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4516    0.1369   -0.1842 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2228   -0.4818   -2.0260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7775    2.2035   -0.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2120    1.4362    0.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6439    0.8552   -1.4100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    0.6013    1.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -0.9821    0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5549   -1.7904    0.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601   -1.5399   -0.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2973    1.4089   -0.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2625    0.1379   -1.5815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7611   -1.6174   -0.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7293    0.4303    1.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6831   -1.0230    1.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8476    1.0919   -0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9601   -0.5081    0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  2  0
  1 10  1  0
  1 11  1  0
  1 12  1  0
  2 13  1  0
  3 14  1  0
  3 15  1  0
  3 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  0
  6 20  1  0
  6 21  1  0
  8 22  1  0
  8 23  1  0
M  END
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PDB for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.976   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.976   3.644   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.311   2.104   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       4.977  -0.206   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0       3.644   3.644   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    5                                                            
MASTER        0    0    0    0    0    0    0    0    9    0   16    0
END
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3D PDB for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

COMPND    HMDB0247199
HETATM    1  C1  UNL     1      -2.334   1.233  -0.424  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.365   0.257   0.247  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.981  -1.101   0.197  1.00  0.00           C  
HETATM    4  C4  UNL     1      -0.067   0.363  -0.512  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.998  -0.545   0.033  1.00  0.00           C  
HETATM    6  N1  UNL     1       1.306  -0.264   1.388  1.00  0.00           N  
HETATM    7  C6  UNL     1       2.234  -0.302  -0.781  1.00  0.00           C  
HETATM    8  N2  UNL     1       3.452   0.137  -0.184  1.00  0.00           N  
HETATM    9  O1  UNL     1       2.223  -0.482  -2.026  1.00  0.00           O  
HETATM   10  H1  UNL     1      -1.778   2.203  -0.542  1.00  0.00           H  
HETATM   11  H2  UNL     1      -3.212   1.436   0.190  1.00  0.00           H  
HETATM   12  H3  UNL     1      -2.644   0.855  -1.410  1.00  0.00           H  
HETATM   13  H4  UNL     1      -1.274   0.601   1.293  1.00  0.00           H  
HETATM   14  H5  UNL     1      -3.060  -0.982   0.511  1.00  0.00           H  
HETATM   15  H6  UNL     1      -1.555  -1.790   0.977  1.00  0.00           H  
HETATM   16  H7  UNL     1      -1.960  -1.540  -0.802  1.00  0.00           H  
HETATM   17  H8  UNL     1       0.297   1.409  -0.376  1.00  0.00           H  
HETATM   18  H9  UNL     1      -0.263   0.138  -1.582  1.00  0.00           H  
HETATM   19  H10 UNL     1       0.761  -1.617  -0.089  1.00  0.00           H  
HETATM   20  H11 UNL     1       0.729   0.430   1.863  1.00  0.00           H  
HETATM   21  H12 UNL     1       1.683  -1.023   1.947  1.00  0.00           H  
HETATM   22  H13 UNL     1       3.848   1.092  -0.385  1.00  0.00           H  
HETATM   23  H14 UNL     1       3.960  -0.508   0.467  1.00  0.00           H  
CONECT    1    2   10   11   12
CONECT    2    3    4   13
CONECT    3   14   15   16
CONECT    4    5   17   18
CONECT    5    6    7   19
CONECT    6   20   21
CONECT    7    8    9    9
CONECT    8   22   23
END
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SMILES for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

CC(C)CC(N)C(N)=O
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INCHI for HMDB0247199 ((S)-2-Amino-4-methylpentanamide)

InChI=1S/C6H14N2O/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H2,8,9)
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
LeucinamideMeSH
Leucinamide monoacetate, (S)-isomerMeSH
Leucinamide monohydrochloride, (S)-isomerMeSH
Leucinamide monohydrochloride, (+-)-isomerMeSH
Leucinamide, (+-)-isomerMeSH
L-Leucine amideMeSH
Chemical FormulaC6H14N2O
Average Molecular Weight130.191
Monoisotopic Molecular Weight130.110613079
IUPAC Name2-amino-4-methylpentanamide
Traditional Name2-amino-4-methylpentanamide
CAS Registry NumberNot Available
SMILES
CC(C)CC(N)C(N)=O
InChI Identifier
InChI=1S/C6H14N2O/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H2,8,9)
InChI KeyFORGMRSGVSYZQR-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentLeucine and derivatives
Alternative Parents
Substituents
  • Leucine or derivatives
  • Alpha-amino acid amide
  • Fatty amide
  • Fatty acyl
  • Carboxamide group
  • Primary carboxylic acid amide
  • Organopnictogen compound
  • Organic nitrogen compound
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Primary aliphatic amine
  • Organic oxygen compound
  • Carbonyl group
  • Amine
  • Hydrocarbon derivative
  • Organic oxide
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
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
logP-0.51ALOGPS
logP-0.13ChemAxon
logS-0.12ALOGPS
pKa (Strongest Acidic)16.69ChemAxon
pKa (Strongest Basic)8.44ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area69.11 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity35.99 m³·mol⁻¹ChemAxon
Polarizability14.69 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
DeepCCS[M+H]+140.53930932474
DeepCCS[M-H]-138.46730932474
DeepCCS[M-2H]-174.24430932474
DeepCCS[M+Na]+149.06630932474
AllCCS[M+H]+131.932859911
AllCCS[M+H-H2O]+127.832859911
AllCCS[M+NH4]+135.732859911
AllCCS[M+Na]+136.832859911
AllCCS[M-H]-130.332859911
AllCCS[M+Na-2H]-133.132859911
AllCCS[M+HCOO]-136.332859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 20229.6641 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20225.32 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid754.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid302.9 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid86.3 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid176.1 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid65.2 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid294.6 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid275.9 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)591.8 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid659.4 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid156.0 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid794.5 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid175.1 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid217.1 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate499.6 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA477.9 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water174.2 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(S)-2-Amino-4-methylpentanamideCC(C)CC(N)C(N)=O2064.2Standard polar33892256
(S)-2-Amino-4-methylpentanamideCC(C)CC(N)C(N)=O1108.7Standard non polar33892256
(S)-2-Amino-4-methylpentanamideCC(C)CC(N)C(N)=O1234.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(N)=O1341.3Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(N)=O1258.6Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(N)=O2062.7Standard polar33892256
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C1295.4Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C1273.3Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C2028.3Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(=O)N[Si](C)(C)C1392.5Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(=O)N[Si](C)(C)C1393.5Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #1CC(C)CC(N[Si](C)(C)C)C(=O)N[Si](C)(C)C1596.6Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C)[Si](C)(C)C1512.3Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C)[Si](C)(C)C1470.7Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C)[Si](C)(C)C1899.4Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C)[Si](C)(C)C1394.0Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C)[Si](C)(C)C1486.9Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C)[Si](C)(C)C1777.3Standard polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1565.7Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1532.5Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1604.3Standard polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #2CC(C)CC(N[Si](C)(C)C)C(=O)N([Si](C)(C)C)[Si](C)(C)C1481.0Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #2CC(C)CC(N[Si](C)(C)C)C(=O)N([Si](C)(C)C)[Si](C)(C)C1536.9Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TMS,isomer #2CC(C)CC(N[Si](C)(C)C)C(=O)N([Si](C)(C)C)[Si](C)(C)C1565.6Standard polar33892256
(S)-2-Amino-4-methylpentanamide,4TMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1732.8Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,4TMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1687.3Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,4TMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1553.2Standard polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(N)=O1579.8Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(N)=O1475.5Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(N)=O2192.4Standard polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C(C)(C)C1524.3Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C(C)(C)C1486.4Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,1TBDMS,isomer #2CC(C)CC(N)C(=O)N[Si](C)(C)C(C)(C)C2151.9Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N[Si](C)(C)C(C)(C)C1817.6Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N[Si](C)(C)C(C)(C)C1826.0Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #1CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N[Si](C)(C)C(C)(C)C1841.2Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1898.6Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1858.6Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #2CC(C)CC(C(N)=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2042.8Standard polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1840.4Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1869.1Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,2TBDMS,isomer #3CC(C)CC(N)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1942.7Standard polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2192.1Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2146.4Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #1CC(C)CC(C(=O)N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1960.4Standard polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #2CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2146.7Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #2CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2136.7Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,3TBDMS,isomer #2CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1939.6Standard polar33892256
(S)-2-Amino-4-methylpentanamide,4TBDMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2514.6Semi standard non polar33892256
(S)-2-Amino-4-methylpentanamide,4TBDMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2450.4Standard non polar33892256
(S)-2-Amino-4-methylpentanamide,4TBDMS,isomer #1CC(C)CC(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2021.6Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (S)-2-Amino-4-methylpentanamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9000000000-7027aee538782f2f03402021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (S)-2-Amino-4-methylpentanamide 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 - (S)-2-Amino-4-methylpentanamide 10V, Positive-QTOFsplash10-000i-9300000000-2de2740441eaff682c3b2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-2-Amino-4-methylpentanamide 20V, Positive-QTOFsplash10-014r-9000000000-c4cf075dcc3e2a2a407e2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-2-Amino-4-methylpentanamide 40V, Positive-QTOFsplash10-0006-9000000000-859ad3ebd25c71295d782021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-2-Amino-4-methylpentanamide 10V, Negative-QTOFsplash10-004i-0900000000-a8f87f6f50d10e6a249c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-2-Amino-4-methylpentanamide 20V, Negative-QTOFsplash10-0006-9200000000-514a7d714f7cec694f002021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-2-Amino-4-methylpentanamide 40V, Negative-QTOFsplash10-0006-9000000000-90726b17dc36e29c52992021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
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 ID102651
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound114616
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. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]