| Weight | 184.964 g/mol |
|---|---|
| Formula | C2H4INO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
iodoacetamide (144-48-9)
Score:
#2369 in Biochemistry
,
#4683 in Biology
,
#5948 in Chemistry
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- Sigma-Aldrich - iodoacetamide43.70 - 803.90 USD
- Fisher Scientific - Search for iodoacetamide
- TCI - iodoacetamide18.00 - 560.00 USD
- Fluorimetry study of N-(1-pyrenyl)iodoacetamide-labelled F-actin. Local structural change of actin protomer both on polymerization and on binding of heavy meromyosin. (FEBS Journal, 2005)
- Elimination of point streaking on silver stained two-dimensional gels by addition of iodoacetamide to the equilibration buffer (Electrophoresis, 1987)
- Iodoacetamide-induced artifact mimics ubiquitination in mass spectrometry (Nature Methods, 2008)
- The use of actin labelled with N-(1-pyrenyl)iodoacetamide to study the interaction of actin with myosin subfragments and troponin/tropomyosin. (Biochemical Journal, 1985)
- Mercuric reductase: homology to glutathione reductase and lipoamide dehydrogenase. Iodoacetamide alkylation and sequence of the active site peptide (Biochemistry, 1983)
- Overalkylation of a Protein Digest with Iodoacetamide (Analytical Chemistry, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)N)I
-
InChIKeyPGLTVOMIXTUURA-UHFFFAOYSA-N
- Pubchem - iodoacetamide
- Wikipedia - iodoacetamide
2-Iodoacetamide is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate. It is commonly used to bind covalently with the thiol group of cysteine so the protein cannot form disulfide bonds.
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