Products for Research Use Only
RegisterLogin

Acetohydroxamic acid

CAT: 0804-HY-B1235-03Size: 500 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0804-HY-B1235-03Size:500 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Acetohydroxamic acid is the inhibitor for bacterial and plant urease that can be used for chronic urinary tract infections. Acetohydroxamic acid selectively inhibits arachidonic acid 5-lipoxygenase that is useful in the research of asthma. Acetohydroxamic acid inhibits the formation of advanced glycation end products, and reduces oxidative stress and inflammatory responses. Acetohydroxamic acid exhibits antiviral activity against HIV[1][2][3].
CAS Number
546-88-3
Product Name Alternative
N-Hydroxyacetamide
UNSPSC
12352211
Hazard Statement
H360
Target
Bacterial; HIV
Type
Reference compound
Related Pathways
Anti-infection
Applications
COVID-19-immunoregulation
Field of Research
Infection; Inflammation/Immunology
Assay Protocol
https://www.medchemexpress.com/Acetohydroxamic-acid.html
Concentration
10mM
Purity
98.66
Solubility
DMSO : 233.33 mg/mL (ultrasonic) |H2O : 100 mg/mL (ultrasonic)
Smiles
CC(NO)=O
Molecular Formula
C2H5NO2
Molecular Weight
75.07
Precautions
H360
References & Citations
[1]Sharma M, et al. Biotransformation of Acetamide to Acetohydroxamic Acid at Bench Scale Using Acyl Transferase Activity of Amidase of Geobacillus pallidus BTP-5x MTCC 9225. Indian J Microbiol. 2012 Mar;52 (1) :76-82.|[2]Umamaheshwari RB, et al., Receptor-mediated targeting of lipobeads bearing acetohydroxamic acid for eradication of Helicobacter pylori. J Control Release. 2004 Sep 14;99 (1) :27-40.|[3]Liu YH, et al., Antiglycation, radical scavenging, and semicarbazide-sensitive amine oxidase inhibitory activities of acetohydroxamic acid in vitro. Drug Des Devel Ther. 2017 Jul 13;11:2139-2147.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched

Chemical Information

Acetohydroxamic Acid

Acetohydroxamic Acid can cause developmental toxicity according to state or federal government labeling requirements.

CAS Number546-88-3
PubChem CID1990
IUPAC NameN-hydroxyacetamide
Molecular FormulaC2H5NO2
Molecular Weight75.07
XLogP-1.6
Topological Polar Surface Area49.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Heavy Atom Count5
Formal Charge0
Complexity42
SMILES
CC(=O)NO
InChI
InChI=1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4)
InChIKey
RRUDCFGSUDOHDG-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Acetohydroxamic Acid
CAS: 546-88-3
CID: 1990
Formula: C2H5NO2
MW: 75.07
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight75.07
XLogP3-1.6
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass75.032028402
Monoisotopic Mass75.032028402
Topological Polar Surface Area49.3 Ų
Heavy Atom Count5
Formal Charge0
Complexity42.9
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

Related Products

CatalogName
HY-140589Acid-PEG4-S-PEG4-acid
HY-140112-01Acid-PEG2-SS-PEG2-acid
HY-140113-01Acid-PEG3-SS-PEG3-acid
HY-W096114-01Acid-PEG8-S-S-PEG8-acid
HY-140114-01Acid-PEG4-S-S-PEG4-acid
HY-N8563Masticadienonic acid
HY-N8543Gliocladic acid
HY-N17650Salviamarinic acid A
HY-N16388α-Costic acid
HY-N15317-01Phocaecholic acid

Alternative Products

CatalogName
A0200-91-01Acetohydroxamic Acid
A16157-1000Acetohydroxamic acid 1g
A16157-100Acetohydroxamic acid 100mg
A16157-500Acetohydroxamic acid 500mg
A16157-10mM-DAcetohydroxamic acid 10mM * 1mL in DMSO
OR1071368-01Acid-apeg6-acid

Popular Products