General Information of Drug (ID: DMYX7NI)

Drug Name
Acetohydroxamic Acid Drug Info
Synonyms
AHA; Acethydroxamsaeure; Acethydroxamsaure; Acetohydroxamate; HAE; Lithostat; Acethydroxamic acid; Acethydroxamsaeure [German]; Acetohydroximic acid; Acetyl hydroxyamino; Acetylhydroxamic acid; Acide acetohydroxamique; Acide acetohydroxamique [French]; Acido acetohidroxamico; Acido acetohidroxamico [Spanish]; Acidum acetohydroxamicum; Acidum acetohydroxamicum [Latin]; Cetohyroxamic acid; Methylhydroxamic acid; SJX HLdmMAH; AHA (TN); Acetic acid, oxime; Acetohydroxamic acid [USAN:INN]; Lithostat (TN); N-Acetyl hydroxyacetamide; N-Acetylhydroxylamine; N-Hydroxyacetamide; N-hydroxyacetimidic acid; N-hydroxyethanimidic acid; S14-0751; Acetohydroxamic acid (USP/INN); Acetamide, N-hydroxy-(9CI)
Indication
Disease Entry ICD 11 Status REF
Urinary tract infection GC08 Approved [1]
Therapeutic Class
Antiinfective Agents
Cross-matching ID
PubChem CID
1990
ChEBI ID
CHEMBL27777
CAS Number
CAS 546-88-3
TTD Drug ID
DMYX7NI
ACDINA Drug ID
D00805

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
3-(4-bromobenzyl)-1,1-dimethylselenourea DMAKMIJ Discovery agent N.A. Investigative [3]
1-cyclohexyl-1-isopropyl-3,3-dimethylselenourea DMS10LE Discovery agent N.A. Investigative [3]
3-dodecyl-1,1-dimethylthiourea DMO5EBI Discovery agent N.A. Investigative [3]
N-glycylglycinehydroxamic acid DMPEZHC Discovery agent N.A. Investigative [4]
3-(4-bromophenyl)-1,1-dimethylthiourea DMXMZRE Discovery agent N.A. Investigative [3]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Bacterial Urease (Bact ureC) TTAS2UO URE1_KLEAE Inhibitor [2]

References

1 FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (NDA) 018749.
2 Enzymatic, immunological and phylogenetic characterization of Brucella suis urease. BMC Microbiol. 2008 Jul 19;8:121.
3 Facile one-pot synthesis of thio and selenourea derivatives: a new class of potent urease inhibitors. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6387-91.
4 Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases. J Med Chem. 2008 Sep 25;51(18):5736-44.