Page last updated: 2024-11-06

janus green b

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

Description

Janus Green B is a redox indicator and a vital stain. It is a lipophilic cationic dye that accumulates in mitochondria, staining them green in living cells. Its synthesis involves the reaction of diethylaminoazobenzene with dimethylaniline in the presence of an oxidizing agent. The dye is a powerful mitochondrial stain, enabling visualization of mitochondrial morphology and function. Janus Green B is used in research to study mitochondrial activity, oxidative stress, and cell viability. It is also employed in histological staining techniques to differentiate various cell types.'

Janus Green B: used in electrodeposition of copper; RN given refers to chloride; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID76123
CHEBI ID21184
SCHEMBL ID285454
MeSH IDM0046402

Synonyms (47)

Synonym
phenazinium, 3-(diethylamino)-7-[[4-(dimethylamino)phenyl]azo]-5-phenyl-, chloride
unii-b9kq101khx
phenazinium, 3-(diethylamino)-7-(2-(4-(dimethylamino)phenyl)diazenyl)-5-phenyl-, chloride (1:1)
b9kq101khx ,
c.i. 11050
nsc-13986
janus green b
janus green v
2869-83-2
nsc13986
phenazinium, 3-(diethylamino)-7-((4-(dimethylamino)phenyl)azo)-5-phenyl-, chloride
einecs 220-695-6
3-(diethylamino)-7-((p-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
3-(diethylamino)-7-((4-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
phenazinium, 3-(diethylamino)-7-((p-(dimethylamino)phenyl)azo)-5-phenyl-, chloride
nsc 13986
3-(diethylamino)-7-{(e)-[4-(dimethylamino)phenyl]diazenyl}-5-phenylphenazin-5-ium chloride
CHEBI:21184
janus green b chloride
janus green b, certified by the biological stain commission, dye content 65 %
J0002
diazin green s
FT-0627546
AKOS015902962
union green b
3-diethylamino-7-(4-dimethylaminophenylazo)-5-phenylphenazinium chloride
3-(diethylamino)-7-(2-(4-(dimethylamino)phenyl)diazenyl)-5-phenylphenazinium chloride (1:1)
janus green b [mi]
SCHEMBL285454
3-(diethylamino)-7-((4-(dimethylamino)phenyl)diazenyl)-5-phenylphenazin-5-ium chloride
janusgreen b
janusgreenb
mfcd00011758
J-017200
janus green b, > 60% dye content
(e)-3-(diethylamino)-7-((4-(dimethylamino)phenyl)diazenyl)-5-phenylphenazin-5-ium chloride
DTXSID80883898
Q418288
janus green b certified
AMY22392
8-[[4-(dimethylamino)phenyl]diazenyl]-n,n-diethyl-10-phenylphenazin-10-ium-2-amine;chloride
D91221
MS-29488
phenazinium, 3-(diethylamino)-7-[2-[4-(dimethylamino)phenyl]diazenyl]-5-phenyl-, chloride (1:1)
HY-D1122
CS-0133970
AKOS040744496

Research Excerpts

Overview

Janus green B (JG-B) is a supravital lipophilic cationic dye which, in its oxidized form, has a green-blue color. It was found to be a specific inhibitor of mitochondrial function in yeast.

ExcerptReferenceRelevance
"Janus green B (JG-B) is a supravital lipophilic cationic dye which, in its oxidized form, has a green-blue color."( Simple, reliable, and time-efficient colorimetric method for the assessment of mitochondrial function and toxicity.
Ahmad, F; Alamoudi, W; Alsamman, K; Haque, S; Salahuddin, M, 2018
)
1.2
"Janus green B was found to be a specific inhibitor of mitochondrial function in yeast. "( Janus green resistance in Saccharomyces cerevisiae: interaction of nuclear and cytoplasmic factors.
Kruszewska, A; Szcześniak, B, 1978
)
1.7
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
dyenull
[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 (37)

TimeframeStudies, This Drug (%)All Drugs %
pre-199023 (62.16)18.7374
1990's2 (5.41)18.2507
2000's6 (16.22)29.6817
2010's6 (16.22)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: 55.24

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 Index55.24 (24.57)
Research Supply Index3.69 (2.92)
Research Growth Index4.49 (4.65)
Search Engine Demand Index86.78 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (55.24)

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%
Other39 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]