Page last updated: 2024-12-05

furothiazole

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

Furothiazole is a synthetic antibacterial drug that has been used to treat bacterial infections. It is a thiazole derivative and acts as a potent inhibitor of bacterial protein synthesis. The compound has been shown to be effective against a wide range of bacteria, including gram-positive and gram-negative species. However, its use is limited due to potential side effects, such as nephrotoxicity. Furothiazole is also used in research to study the mechanism of action of antibiotics and to develop new antibacterial agents.'

furothiazole: carcinogen for mouse, rat, dog, hamster; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID10753
CHEMBL ID259186
CHEBI ID82353
SCHEMBL ID3824030
MeSH IDM0046808

Synonyms (32)

Synonym
531-82-8
n-[4-(5-nitrofuran-2-yl)-1,3-thiazol-2-yl]acetamide
n-[4-(5-nitro-2-furyl)-2-thiazolyl]acetamide
thiazole, 2-acetylamino-4-(5-nitro-2-furyl)-
brn 0544226
acetamide, n-(4-(5-nitro-2-furanyl)-2-thiazolyl)-
furothiazole
acetamide, n-(4-(5-nitro-2-furyl)-2-thiazolyl)-
furathiazole
thiazole, 2-acetamido-4-(5-nitro-2-furyl)-
2-acetamino-4-(5-nitro-2-furyl)thiazole
n-(4-(5-nitro-2-furanyl)-2-thiazolyl)acetamide
thiazole, 2-acetamino-4-(5-nitro-2-furyl)-
2-acetylamino-4-(5-nitro-2-furyl)thiazole
2-acetamido-4-(5-nitro-2-furyl)thiazole
nfta
as17665 ,
furium
ccris 446
n-(4-(5-nitro-2-furyl)-2-thiazolyl)acetamide
chebi:82353 ,
CHEMBL259186
C19273
q42hoe346s ,
unii-q42hoe346s
n-(4-(5-nitro-2-furyl)-2-thiazolyl)acetamide [iarc]
bactofuril
SCHEMBL3824030
DTXSID9020952
acetamide, n-[4-(5-nitro-2-furanyl)-2-thiazolyl]-
n-(4-(5-nitrofuran-2-yl)thiazol-2-yl)acetamide
Q27155894

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
"54 in ascending dosage order beginning with 100 ppm."( Suppression of antibody-mediated and cell-mediated murine immunity by the carcinogen N-[4-(5-nitro-2-furyl)-2-thiazolyl]acetamide.
Bryan, GT; Cohen, SM; Headley, DB, 1977
)
0.26
" The radioactivity level in the visceral organs reached a maximum 2 hr after dosing and then gradually decreased."( Metabolism and disposition of N-(4-(5-nitro-2-furyl)-(2-14-C)thiazolyl)acetamide in the rat.
Bryan, GT; Chiu, CW; Wang, CY,
)
0.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aromatic amideAn amide in which the amide linkage is bonded directly to an aromatic system.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID318681Anticarcinogenic activity in rat assessed as induction of tumors per day2008Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
QSAR modeling of the rodent carcinogenicity of nitrocompounds.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (71.43)18.7374
1990's0 (0.00)18.2507
2000's1 (14.29)29.6817
2010's0 (0.00)24.3611
2020's1 (14.29)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]