xylidyl blue i

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

Description

xylidyl blue I: RN from Chem Abstracts Index Guide 1984; RN not in Chemline 5/84 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID Source	ID
PubMed CID	135442960
SCHEMBL ID	2861735
MeSH ID	M0121485

Synonyms (22)

Synonym
xylidyl blue i
einecs 239-012-8
14936-97-1
1-azo-2-hydroxy-3-(2,4-dimethylcarboxyanilido)naphthalene-1'-(2-hydroxybenzene-5-sulfonic acid) sodium salt
2-[2-hydroxy-3-(2,4-xylylcarbamoyl)-1-naphthylazo]-1-phenol-4-sulfonic acid sodium salt
sodium 3-((3-(((2,4-dimethylphenyl)amino)carbonyl)-2-hydroxy-1-naphthyl)azo)-4-hydroxybenzenesulphonate
magonsulfonate
FT-0637162
SCHEMBL2861735
AKOS024285054
xylidyl blue i sodium salt
J-610035
mfcd00003890
xb-i; magonsulfonate
sodium (e)-3-((3-(2,4-dimethylphenylcarbamoyl)-2-hydroxynaphthalen-1-yl)diazenyl)-4-hydroxybenzenesulfonate
T70316
xylylazo violet i [spectrophotometric reagent for mg]
sodium3-(2-(3-((2,4-dimethylphenyl)carbamoyl)-2-oxonaphthalen-1(2h)-ylidene)hydrazineyl)-4-hydroxybenzenesulfonate
2321383-50-8
sodium 3-(2-(3-((2,4-dimethylphenyl)carbamoyl)-2-oxonaphthalen-1(2h)-ylidene)hydrazineyl)-4-hydroxybenzenesulfonate
sodium;3-[[3-[(2,4-dimethylphenyl)carbamoyl]-2-hydroxynaphthalen-1-yl]diazenyl]-4-hydroxybenzenesulfonate
SODIUM (E)-3-((3-((2,4-DIMETHYLPHENYL)CARBAMOYL)-2-HYDROXYNAPHTHALEN-1-YL)DIAZENYL)-4-HYDROXYBENZENESULFONATE

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	3 (60.00)	18.7374
1990's	2 (40.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	0 (0.00%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	5 (100.00%)	84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Substance	Relationship Strength	Studies	Classes	Roles
citric acid, anhydrous Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.. citric acid : A tricarboxylic acid that is propane-1,2,3-tricarboxylic acid bearing a hydroxy substituent at position 2. It is an important metabolite in the pathway of all aerobic organisms.	1.99	1	tricarboxylic acid	antimicrobial agent; chelator; food acidity regulator; fundamental metabolite
calmagite calmagite: indicator used to measure free magnesium &/or calcium in biological systems; structure	1.96	1
bromthymol blue Bromthymol Blue: A pH sensitive dye that has been used as an indicator in many laboratory reactions.. bromothymol blue : A member of the class of 2,1-benzoxathioles that is 2,1-benzoxathiole 1,1-dioxide in which both of the hydrogens at position 3 have been substituted by 3-bromo-4-hydroxy-5-isopropyl-2-methylphenyl groups.	1.96	1	2,1-benzoxathiole; arenesulfonate ester; organobromine compound; polyphenol; sultone	acid-base indicator; dye; two-colour indicator
methylthymol blue methylthymol blue: RN given refers to tetra-Na salt	1.96	1
titan yellow titan yellow: RN given refers to di-Na salt	1.96	1
nadp [no description available]	1.99	1
chiniofon Hydroxyquinolines: The 8-hydroxy derivatives inhibit various enzymes and their halogenated derivatives, though neurotoxic, are used as topical anti-infective agents, among other uses.	1.96	1

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