Record Information
Version1.0
Creation date2015-10-09 22:32:40 UTC
Update date2017-01-19 02:36:36 UTC
FoodComEx IDPC000789
FoodDB RecordFDB022372
Chemical Information
NameN-Formyl-L-methionine
DescriptionEffective in the initiation of protein synthesis. The initiating methionine residue enters the ribosome as N-formylmethionyl tRNA. This process occurs in Escherichia coli and other bacteria as well as in the mitochondria of eucaryotic cells. [HMDB]
CAS Number4289-98-9
Structure
Thumb
Synonyms
SynonymSource
fMethmdb
For-Met-OHhmdb
Formyl-L-methioninehmdb
formylmethioninehmdb
N-Formyl-L-methioninehmdb
N-formyl-methioninehmdb
Chemical FormulaC6H11NO3S
IUPAC name(2R)-2-formamido-4-(methylsulfanyl)butanoic acid
InChI IdentifierInChI=1S/C6H11NO3S/c1-11-3-2-5(6(9)10)7-4-8/h4-5H,2-3H2,1H3,(H,7,8)(H,9,10)/t5-/m1/s1
InChI KeyPYUSHNKNPOHWEZ-RXMQYKEDSA-N
Isomeric SMILESCSCC[C@@H](NC=O)C(O)=O
Average Molecular Weight177.221
Monoisotopic Molecular Weight177.045963913
Chemical Taxonomy
Description Belongs to the class of organic compounds known as methionine and derivatives. Methionine and derivatives are compounds containing methionine or a derivative thereof resulting from reaction of methionine 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 ParentMethionine and derivatives
Alternative Parents
Substituents
  • Methionine or derivatives
  • N-formyl-alpha-amino acid
  • N-formyl-alpha amino acid or derivatives
  • Thia fatty acid
  • Fatty acyl
  • Fatty acid
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Thioether
  • Sulfenyl compound
  • Dialkylthioether
  • Organosulfur compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointNot Available
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 200 mg
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci V5922
MetaSci HMDB0001015
Sigma-Aldrich HMDB0001015
Toronto Research Chemicals F700693