Page last updated: 2024-12-05

nile blue

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

Description

Nile blue is a fluorescent dye that has been used for various applications in research, including staining of biological samples, studying cell function, and detecting various chemical compounds. It is synthesized by reacting a mixture of nitrosodimethylaniline, aniline, and concentrated sulfuric acid. Nile blue exhibits different colors in different pH environments, making it useful for observing changes in acidity within cells. It is also known to be effective in staining nucleic acids, including DNA and RNA, which allows researchers to study the structure and function of these important biomolecules. The dye's fluorescent properties make it suitable for microscopy and imaging techniques, allowing scientists to visualize and analyze biological samples with high sensitivity. Furthermore, nile blue has been explored for its potential therapeutic applications, such as its use in diagnosing and treating certain medical conditions. Its research interest stems from its ability to interact with biological systems in unique ways, providing valuable insights into cellular processes, disease mechanisms, and potential treatment strategies.'

Nile Blue: RN given refers to chloride; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

nile blue A : An organic chloride salt having 5-amino-9-(diethylamino)benzo[a]phenoxazin-7-ium as the couterion. fluorescent dye which is also a potent photosensitiser for photodynamic therapy. [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]

Cross-References

ID SourceID
PubMed CID16938
CHEMBL ID407862
CHEBI ID52163
SCHEMBL ID344996
SCHEMBL ID26061
MeSH IDM0052622

Synonyms (59)

Synonym
einecs 219-181-4
nsc 146184
benzo(a)phenazoxonium, 5-amino-9-(diethylamino)-, chloride
5-amino-9-(diethylamino)benzo(a)phenoxazin-7-ium chloride
benzo(a)phenoxazin-7-ium, 5-amino-9-(diethylamino)-, chloride
5h-benzo(a)phenazoxazine, 9-diethylamino-5-imino-, hydrochloride
nile blue hydrochloride
basic blue 12
nsc-146184
cresol fast violet
nile blue chloride
nile blue base
c.i. basic blue 12
5h-benzo[a]phenazoxazine, sulfate (2:1)
c.i. 51180
2381-85-3
nile blue a
benzo[a]phenoxazin-7-ium, sulfate (2:1)
nile blue ax
5h-benzo[a]phenazoxazine, hydrochloride
wln: t d6 b666 cn joj gn2&2 mz &g &15/28
nsc146184
nile blue
cresyl fast violet
nile blue chloride, dye content 85 %
benzo(a)phenazoxonium, 5-amino-9-(diethylamino)-,chloride
CHEBI:52163
5-amino-9-(diethylamino)benzo[a]phenoxazin-7-ium chloride
CHEMBL407862
N0317
AKOS004901544
AKOS004901433
e58rl8t2x3 ,
benzo(a)phenoxazin-7-ium, 5-amino-9-(diethylamino)-, chloride (1:1)
unii-e58rl8t2x3
SCHEMBL344996
SCHEMBL26061
benzo[a]phenoxazin-7-ium, 5-amino-9-(diethylamino)-, chloride
mfcd00011936
basic blue 12 (nile blue hydrochloride)
nile blue a chloride
AKOS024353698
basic blue 12 (c.i. 51180)
nile blue chloride, for fluorescence
J-015226
n-(5-amino-9h-benzo[a]phenoxazin-9-ylidene)-n-ethylethanaminium chloride
FT-0759287
DTXSID40883834
5-isopropyl-1-methyl-1h-pyrazole-3-carboxylicacid
Q27123279
D91676
BS-32169
12-amino-n,n-diethyl-8h-10-oxa-5-azatetraphen-8-iminium chloride
(5-aminobenzo[a]phenoxazin-9-ylidene)-diethylazanium;chloride
CS-0169074
HY-W110898
9-n,n-diethylamino-5-iminobenzo(a)phenoxazine monohydrochloride
benzo[a]phenoxazin-7-ium,5-amino-9-(diethylamino)-,chloride(1:1)
SY074371

Research Excerpts

Overview

Nile Blue is a red-emissive dye that is well-known for imaging and staining applications. Nile blue A appears to be a more specific stain for poly-beta-hydroxybutyrate than Sudan black B.

ExcerptReferenceRelevance
"Nile Blue (NB) is a red-emissive dye that is well-known for imaging and staining applications. "( Nile Blue: A Red-Emissive Fluorescent Dye That Displays Differential Self-Assembly and Binding to G-Quadruplexes.
M, M; Patidar, RK; Ranjan, N; Srivastava, N; Tiwari, R, 2023
)
3.8

Effects

ExcerptReferenceRelevance
"Nile blue derivatives have been shown to be potentially effective photosensitizers for photodynamic therapy of malignant tumors. "( Lysosomal localization and mechanism of uptake of Nile blue photosensitizers in tumor cells.
Cincotta, L; Foley, JW; Kirley, SD; Lin, CW; Shulok, JR, 1991
)
1.98

Compound-Compound Interactions

ExcerptReferenceRelevance
"An innovative surface-enhanced Raman spectroscopy and lateral flow assay (SERS-LFA) biosensor combined with aptamer recognition had been developed for the convenient, rapid, sensitive and accurate detection of thrombin and platelet-derived growth factor-BB (PDGF-BB) associated with prostate cancer simultaneously."( A SERS-LFA biosensor combined with aptamer recognition for simultaneous detection of thrombin and PDGF-BB in prostate cancer plasma.
Cao, X; Li, L; Lu, W; Mao, Y; Song, Q; Sun, Y, 2021
)
0.62
"In this study, we reported a novel sensing platform based on fluorescence quenching composed of alendronic acid (ADA) coated upconversion nanoparticles (UCNPs) and Nile Blue (NB) combined with polymerase chain reaction (PCR) for rapid, sensitive, and specific detection of Escherichia coli (E."( A novel ADA-coated UCNPs@NB sensing platform combined with nucleic acid amplification for rapid detection of Escherichia coli.
Chen, M; Han, L; Pan, L; Song, Y; Tu, K; Yan, Z, 2023
)
1.11

Dosage Studied

ExcerptRelevanceReference
"The recovery studies in both pharmaceutical dosage forms and urine showed that the proposed method ensured good selectivity, precision and accuracy without any interference from inactive excipients."( Voltammetric Analysis of Ephedrine in Pharmaceutical Dosage Forms and Urine Using poly(Nile Blue A) Modified Glassy Carbon Electrode.
Ağın, F; Kul, D; Öztürk, G, 2021
)
0.84
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID598438Selectivity index, ratio of IC50 for rat L6 cells to IC50 for Plasmodium falciparum K12010ACS medicinal chemistry letters, Oct-14, Volume: 1, Issue:7
Discovery of Novel Benzo[a]phenoxazine SSJ-183 as a Drug Candidate for Malaria.
AID598437Cytotoxicity against rat L6 cells2010ACS medicinal chemistry letters, Oct-14, Volume: 1, Issue:7
Discovery of Novel Benzo[a]phenoxazine SSJ-183 as a Drug Candidate for Malaria.
AID597500Antimalarial activity against Plasmodium berghei NK-65 infected in ICR mouse assessed as inhibition of parasitemia at 100 mg/kg, po administered as single dose on day 1 measured on day 42010ACS medicinal chemistry letters, Oct-14, Volume: 1, Issue:7
Discovery of Novel Benzo[a]phenoxazine SSJ-183 as a Drug Candidate for Malaria.
AID597501Antimalarial activity against Plasmodium berghei NK-65 infected in ICR mouse assessed as survival days at 100 mg/kg, po administered as single dose (Rvb = 6 days)2010ACS medicinal chemistry letters, Oct-14, Volume: 1, Issue:7
Discovery of Novel Benzo[a]phenoxazine SSJ-183 as a Drug Candidate for Malaria.
AID322909Antifungal activity against Saccharomyces cerevisiae W303-1B after 48 hrs by broth microdilution assay2008Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
Synthesis of naphtho[2,3-a]phenoxazinium chlorides: structure-activity relationships of these heterocycles and benzo[a]phenoxazinium chlorides as new antimicrobials.
AID598436Antimalarial activity against chloroquine and pyrimethamine resistant Plasmodium falciparum K12010ACS medicinal chemistry letters, Oct-14, Volume: 1, Issue:7
Discovery of Novel Benzo[a]phenoxazine SSJ-183 as a Drug Candidate for Malaria.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (212)

TimeframeStudies, This Drug (%)All Drugs %
pre-199046 (21.70)18.7374
1990's25 (11.79)18.2507
2000's49 (23.11)29.6817
2010's72 (33.96)24.3611
2020's20 (9.43)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 64.30

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index64.30 (24.57)
Research Supply Index5.38 (2.92)
Research Growth Index4.73 (4.65)
Search Engine Demand Index195.59 (26.88)
Search Engine Supply Index3.59 (0.95)

This Compound (64.30)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.46%)5.53%
Reviews1 (0.46%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other214 (99.07%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]