Page last updated: 2024-12-07

methylene green

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

Description

Methylene green is a cationic dye with a deep green color. It was first synthesized in 1879 and has been used in various applications, including as a biological stain, a redox indicator, and a therapeutic agent. The synthesis of methylene green typically involves the oxidation of dimethylaniline with potassium dichromate in the presence of sulfuric acid. Methylene green exhibits a variety of effects, including antimicrobial, anti-inflammatory, and antioxidant properties. It has been shown to be effective against various bacterial and fungal infections. In addition, methylene green has been investigated for its potential therapeutic effects in conditions such as Alzheimer's disease, Parkinson's disease, and cancer. Methylene green is studied due to its unique chemical and biological properties, including its ability to act as an electron carrier, its interaction with DNA, and its potential to modulate cellular signaling pathways. Research on methylene green continues to explore its various applications and therapeutic potential.'

methylene green: stain; 4-nitro(methylene blue); RN given refers to chloride [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

methylene green : An organic chloride salt having 3,7-bis(dimethylamino)-4-nitrophenothiazin-5-ium as the counterion. It stains nuclei green and is sometimes used as a counterstain to red or purple primary stains. [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 CID75889
CHEBI ID87675
SCHEMBL ID43823
SCHEMBL ID17591862
MeSH IDM0092041

Synonyms (38)

Synonym
wln: t c666 bn isj fn1&1 gnw ln1&1 &q &g
nsc-9403
phenothiazin-5-ium,7-bis(dimethylamino)-4-nitro-, chloride
c.i. basic green 5
2679-01-8
nsc9403
methylene green (van)
nsc 9403
basic green 5
3,7-bis(dimethylamino)-4-nitrophenothiazin-5-ium chloride
7-(dimethylamino)-6-nitro-3h-phenothiazin-3-ylidene)dimethylammonium chloride
nsc 367083
phenothiazin-5-ium, 3,7-bis(dimethylamino)-4-nitro-, chloride
einecs 220-231-2
c.i. basic green 5 (van)
nsc367083
nsc-367083
methylene green
c.i. 52020
unii-f1io2zp7bu
f1io2zp7bu ,
6722-15-2
ci 52020
AKOS025311082
SCHEMBL43823
CHEBI:87675
AKOS024375417
methylenegreen
SCHEMBL17591862
mfcd00151524
phenothiazin-5-ium, 3,7-bis(dimethylamino)-4-nitro-, chloride (1:1)
(7-(dimethylamino)-6-nitro-3h-phenothiazin-3-ylidene)dimethylammonium chloride
J-016547
Q10858041
[7-(dimethylamino)-4-nitrophenothiazin-3-ylidene]-dimethylazanium;chloride
DTXSID70949598
5,6,7,8-tetrahydro-imidazo[1,2-a]pyrazine-2-carboxylicacid
methylene green complex with half zncl2n

Research Excerpts

Overview

Methylene green is a versatile dye that can be used in a wide range of technical applications, most of which require the dye to be pure.

ExcerptReferenceRelevance
"Methylene green is a versatile dye that can be used in a wide range of technical applications, most of which require the dye to be pure. "( Simple procedures for analyzing and purifying methylene green.
Chesta, CA; Glusko, CA; Montejano, HA; Previtali, CM, 2012
)
2.08
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
fluorochromeA fluorescent dye used to stain biological specimens.
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 chloride 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 (29)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (6.90)18.7374
1990's3 (10.34)18.2507
2000's7 (24.14)29.6817
2010's15 (51.72)24.3611
2020's2 (6.90)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 43.26

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 Index43.26 (24.57)
Research Supply Index3.43 (2.92)
Research Growth Index4.98 (4.65)
Search Engine Demand Index60.29 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.26)

All Compounds (24.57)

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%
Other30 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]