Page last updated: 2024-12-06

anft

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

Description

ANFT: RN given refers to unlabeled cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID38052
CHEMBL ID259567
SCHEMBL ID3344653
MeSH IDM0083598

Synonyms (18)

Synonym
2-amino-4-(5-nitro-2-furyl)thiazole
4-(5-nitrofuran-2-yl)-1,3-thiazol-2-amine
38514-71-5
2-thiazolamine, 4-(5-nitro-2-furanyl)-
ccris 42
anft
brn 0527688
thiazole, 2-amino-4-(5-nitro-2-furyl)-
4-(5-nitro-2-furanyl)-2-thiazolamine
OPREA1_409651
CHEMBL259567
q45kv2an7k ,
unii-q45kv2an7k
SCHEMBL3344653
DTXSID4039237
Q63088097
nitro-2-furanyl)-2-thiazolamine, 4-(5-
EN300-1826113

Research Excerpts

Overview

FANFT is a more potent uroepithelial carcinogen than ANFT. Previous studies have shown extensive deformylation of FANFT to ANFT in vivo. ANFT is the putative proximate carcinogen.

ExcerptReferenceRelevance
"ANFT appears to be a thiyl radical trap."( Mechanism of formation of the thioether conjugate of the bladder carcinogen 2-amino-4-(5-nitro-2-furyl)-thiazole (ANFT).
Davis, BB; Lakshmi, VM; Sohani, S; Zenser, TV, 1992
)
1.22
"FANFT is a more potent uroepithelial carcinogen than ANFT but previous studies have shown extensive deformylation of FANFT to ANFT in vivo and ANFT to be the putative proximate carcinogen."( Metabolism and excretion of nitrofurothiazole bladder carcinogens.
Davis, B; Lakshmi, VM; Spry, L; Zenser, T, 1986
)
0.89

Treatment

ExcerptReferenceRelevance
"The ANFT-treated cells followed by control medium or urea and cells treated with ANFT, NaS and urea were tumorigenic when transplanted to nude mice, whereas NaS or ANFT followed by NaS treatment were not."( In vitro transformation of rat bladder epithelium by 2-amino-4-(5-nitro-2-furyl)thiazole.
Borgeson, CD; Chlapowski, FJ; Cohen, SM; Mann, AM; Masui, T; Okamura, T, 1991
)
0.76

Dosage Studied

ExcerptRelevanceReference
" ANFT-induced ornithine decarboxylase activity was principally localized in the bladder epithelium and was inhibited in a linear dose-response relationship by the synthetic retinoid, 13-cis-retinoic acid."( Early induction of mouse urinary bladder ornithine decarboxylase activity by rodent vesical carcinogens.
Bryan, GT; Matsushima, M, 1980
)
1.17
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

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 (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-199019 (61.29)18.7374
1990's11 (35.48)18.2507
2000's1 (3.23)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 48.10

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index48.10 (24.57)
Research Supply Index3.47 (2.92)
Research Growth Index4.05 (4.65)
Search Engine Demand Index73.11 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (48.10)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.23%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other30 (96.77%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]