| Weight | 177.225 g/mol |
|---|---|
| Formula | C6H11NO3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
N-formyl-L-methionine (4289-98-9)
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- Structure and conformation of amino acids containing sulfur. V. N-Formyl-l-methionine (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1977)
- Peptide models XLV: Conformational properties of NformylLmethioninamide and its relevance to methionine in proteins (Proteins, 2004)
- N-formyl-l-methionine deformylase activity in human leucocytes and platelets (Biochemical Journal, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCSCCC(C(=O)O)NC=O
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InChIKeyPYUSHNKNPOHWEZ-UHFFFAOYSA-N
- Pubchem - N-formyl-L-methionine
- Wikipedia - N-Formylmethionine
N-Formylmethionine (fMet) is a derivative of the amino acid methionine in which a formyl group has been added to the amino group. It is specifically used for initiation of protein synthesis from bacterial and organellar genes, and may be removed post-translationally. fMet plays a crucial part in the protein synthesis of bacteria, mitochondria and chloroplasts.
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N-formyl-L-methionine
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