Page last updated: 2024-12-06

eosine i bluish

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

Description

Eosine I Bluish: A red fluorescein dye used as a histologic stain. It may be cytotoxic, mutagenic, and inhibit certain mitochondrial functions. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12961637
CHEBI ID39077
MeSH IDM0016617

Synonyms (27)

Synonym
dibromodinitrofluorescein sodium
c.i. 45400
saffrosine
eosine bnx
eosine ba
c.i. acid red 91
eosine i bluish
2-(4,5-dibromo-3,6-dihydroxy-2,7-dinitroxanthen-9-yl)-benzoic acid, disodium salt
disodium 4',5'-dibromo-2',7'-dinitro-3-oxo-3h-spiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate
acid red 91
spiro(isobenzofuran-1(3h),9'-(9h)xanthen)-3-one, 4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitro-, disodium salt
CHEBI:39077
eosine bn
eosin ba
oms4xqd1t0 ,
einecs 208-943-1
ai3-63053
unii-oms4xqd1t0
4',5'-dibromo-2',7'-dinitrofluorescein disodium salt
4',5'-dibromo-3',6'-dihydroxy-2',7'-dinitrospiro(isobenzofuran-1(3h),9'-(9h)xanthen)-3-one sodium salt (1:2)
hydroxydibromodinitro-o-carboxyphenylfluorone sodium
eosine i bluish [mi]
AKOS027250850
disodium;4',5'-dibromo-2',7'-dinitro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate
DTXSID00928770
134829-78-0
disodium 4',5'-dibromo-2',7'-dinitro-3-oxo-3h-spiro[2-benzofuran-1,9'-xanthene]-3',6'-bis(olate)

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"5 times more toxic than dimethoate or abamectin, diazinon was less toxic, and phloxine B (a phototoxic dye) least toxic."( Toxicity and residual effectiveness of insecticides on insecticide-treated spheres for controlling females of Rhagoletis pomonella (Diptera: Tephritidae).
Clark, JM; Hu, XP; Prokopy, RJ, 2000
)
0.31
" A series oftests with commercial adjuvants was performed under laboratory conditions that demonstrated a multifold decrease in the LD50 of phloxine B concentration and a decrease in the time required for photodynamic action to kill the flies."( Photoactive dye insecticide formulations: adjuvants increase toxicity to Mexican fruit fly (Diptera: Tephritidae).
Mangan, RL; Moreno, DS, 2001
)
0.31
"Phototoxicity consists in the capability of certain innocuous molecules to become toxic when subjected to suitable illumination."( Reliable Screening of Dye Phototoxicity by Using a Caenorhabditis elegans Fast Bioassay.
Bianchi, JI; Blázquez-Castro, A; Buzz, LI; Buzzi, LI; Simonetta, SH; Stockert, JC, 2015
)
0.42

Bioavailability

ExcerptReferenceRelevance
" Therefore, these studies were performed to determine oral bioavailability and pharmacokinetic parameters of Red 28 in male F-344 rats following single and repeated oral dosing."( Absorption and elimination of D and C Red No. 28 in male F-344 rats.
Sipes, IG; Sólyom, AM; Sweet, CJ, 2004
)
0.32
" This illustrates the importance of profiling for reactive ionogenic substances; even limited bioavailability combined with reactivity can result in exposures to a hazardous substance not predictable by traditional in silico modeling methods."( Estimation of the bioaccumulation potential of a nonchlorinated bisphenol and an ionogenic xanthene dye to Eisenia andrei in field-collected soils, in conjunction with predictive in silico profiling.
Bonnell, M; Princz, J; Ritchie, E; Robidoux, PY; Scroggins, R; Velicogna, J, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
fluorescent dyenull
histological dyeA dye used in microscopic or electron microscopic examination of cells and tissues to give contrast and to highlight particular features of interest, such as nuclei and cytoplasm.
[role 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]

Drug Classes (1)

ClassDescription
organic sodium salt
[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]

Research

Studies (113)

TimeframeStudies, This Drug (%)All Drugs %
pre-199011 (9.73)18.7374
1990's18 (15.93)18.2507
2000's42 (37.17)29.6817
2010's37 (32.74)24.3611
2020's5 (4.42)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 (%)
Trials1 (0.82%)5.53%
Reviews2 (1.64%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other119 (97.54%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]