Compounds > 2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine
Page last updated: 2024-12-06

2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine

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

Description

2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine: has antibacterial activity; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID61579
SCHEMBL ID68355
MeSH IDM0465725

Synonyms (35)

Synonym
pyridine, 4-(methylsulfonyl)-2,3,5,6-tetrachloro-
sa 1013
epa pesticide chemical code 068901
caswell no. 830a
2,3,5,6-tetrachloro-4-(methylsulphonyl)pyridine
pyridine, 2,3,5,6-tetrachloro-4-(methylsulfonyl)-
tetrachloromethylsulfonylpyridine
dowicil s-13
brn 1537517
2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine
4-(methylsulfonyl)-2,3,5,6-tetrachloropyridine
einecs 236-035-5
2,3,5,6-tetrachloro-4-methylsulfonylpyridine
2,3,5,6-tetrachloro-4-(methylsulfonyl) pyridine
2,3,5,6-tetrachloro-4-(methylsulphonyl)pyridine;tetrachloro-4-(methylsulfonyl)pyridine;2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine
A26183
2,3,5,6-tetrochloro-4-(methylsulfonyl)pyridine
13108-52-6
unii-92agr11yjb
92agr11yjb ,
5-21-02-00127 (beilstein handbook reference)
AKOS015913924
tetrachloro-4-(methylsulfonyl)pyridine, 2,3,5,6-
SCHEMBL68355
T3670
DTXSID4044795
methyl 2,3,5,6-tetrachloro-4-pyridyl sulfone
W-108340
c6h3cl4no2s
mfcd00054553
FT-0717242
Q5230387
DS-15470
CS-0150153
2,3,5,6-tetrachloro-4-methanesulfonylpyridine

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" As the respiratory chain is similar in all living organisms, it can be concluded that the toxic effect of TCMS most likely depend on the different bioavailability of the compound and on the different importance of mitochondria in the ATP production in the animal species."( TCMS inhibits ATP synthesis in mitochondria: a systematic analysis of the inhibitory mechanism.
Ballarin, L; Bragadin, M; Cima, F; Iero, A; Manente, S, 2007)		0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's7 (100.00)29.6817
2010's0 (0.00)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: 12.28

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.28 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.36 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.28)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies4 (57.14%)4.05%
Observational0 (0.00%)0.25%
Other3 (42.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
formaldehyde
paraform: polymerized formaldehyde; RN given refers to parent cpd; used in root canal therapy		2.0510aldehyde;
one-carbon compound		allergen;
carcinogenic agent;
disinfectant;
EC 3.5.1.4 (amidase) inhibitor;
environmental contaminant;
Escherichia coli metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
phenoxarsine oxide
phenoxarsine oxide: structure		2.0210
thiazoles
[no description available]		2.02101,3-thiazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene
2-n-octyl-4-isothiazolin-3-one
octhilinone : A member of the class of 1,2-thiazole that is 1,2-thiazol-3-one substituted on the nitrogen (position 2) by an octyl group. A fungicide and antibacterial agent, it is used for treatment of canker and other fungal and bacterial diseases in fruit trees. It is no longer approved for use within the European Union.		2.02101,2-thiazolesantibacterial agent;
antifungal agrochemical;
environmental contaminant;
xenobiotic
arsenic
Arsenic: A shiny gray element with atomic symbol As, atomic number 33, and atomic weight 75. It occurs throughout the universe, mostly in the form of metallic arsenides. Most forms are toxic. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), arsenic and certain arsenic compounds have been listed as known carcinogens. (From Merck Index, 11th ed)		2.0210metalloid atom;
pnictogen		micronutrient
ConditionIndicatedRelationship StrengthStudiesTrials
Allergic Contact Dermatitis
[description not available]		02.9440
Dermatitis, Allergic Contact
A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure.		02.9440
Dermatitis, Occupational
A recurrent contact dermatitis caused by substances found in the work place.		02.7330
Prurigo
A name applied to several itchy skin eruptions of unknown cause. The characteristic course is the formation of a dome-shaped papule with a small transient vesicle on top, followed by crusting over or lichenification. (From Dorland, 27th ed)		02.0410