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iodoacetamide

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EntityQ2191895· pop 14· linked from 19 articles

iodoacetamide

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Also known as 2-iodoacetamide

Iodoacetamide (IAA) is an organic compound with the chemical formula . It 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. It is also used in ubiquitin studies as an inhibitor of deubiquitinase enzymes (DUBs) because it alkylates the cysteine residues at the DUB active site.

In the Vinony graph

Vinony's link graph records 19 inbound references to iodoacetamide, and connects out to iodoacetic acid, hydrogen and oxygen.

Vinony files it under Acetamides, Alkylating agents and ECHA InfoCard ID from Wikidata.

Vinony links it to 13 Wikipedia language editions.

Chemical data

Formula
C2H4INO
Molecular weight
184.96 g/mol
IUPAC name
2-iodoacetamide
SMILES
C(C(=O)N)I
InChIKey
PGLTVOMIXTUURA-UHFFFAOYSA-N
XLogP
-0.2
Polar surface area
43.1 Ų
H-bond donors
1
H-bond acceptors
1
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of
amides
Mass
184.933762
Show 5 more facts
chemical formula
C₂H₄INO
canonical SMILES
C(C(=O)N)I
subject has role
enzyme inhibitor
melting point
93.5
Commons category
Iodoacetamide
Sources (4)

via Wikidata · CC0

~2 min read

Encyclopedic overview

4 sections
Contents
  • Peptidase inhibitor
  • Protein mass spectrometry
  • References
  • External links

Iodoacetamide (IAA) is an organic compound with the chemical formula . It 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. It is also used in ubiquitin studies as an inhibitor of deubiquitinase enzymes (DUBs) because it alkylates the cysteine residues at the DUB active site.

==Peptidase inhibitor== Iodoacetamide is an irreversible inhibitor of all cysteine peptidases, with the mechanism of inhibition occurring from alkylation of the catalytic cysteine residue (see schematic). In comparison with its acid derivative, iodoacetate, iodoacetamide reacts substantially faster. This observation appears contradictory to standard chemical reactivity, however the presence of a favourable interaction between the positive imidazolium ion of the catalytic histidine and the negatively charged carboxyl-group of the iodoacetate is the reason for the increased relative activity of iodoacetamide. thumb|left|500px|Mechanism of irreversible inhibition of cysteine peptidases with iodoacetamide.

Excerpted from Wikipedia’s “iodoacetamide” article, available under the CC BY-SA 4.0 licence.

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