Page last updated: 2024-12-09

2-thiopyridine

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

Description

2-thiopyridine: RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

pyridine-2-thiol : Pyridine substituted at C-2 by a sulfanyl group. [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 CID2723698
CHEMBL ID1235541
CHEBI ID45223
SCHEMBL ID54576
MeSH IDM0093630

Synonyms (76)

Synonym
CHEMBL1235541
2-pyridinethiol
2-thiopyridine
pyrid-2-thione
2-thiopyridone
2637-34-5
wln: t6nj bsh
nsc-41337
2-pyridinethione
nsc41337
2(1h)-pyridinethione
2-mercaptopyridine ,
thiopyridone-2 [french]
nsc 41337
einecs 220-131-9
pyridine-2-thiol
PYS ,
2-mercaptopyridine, reagentplus(r), 99%
DB03329
2-pyridylthiol
2-pyridinylthiol
73018-10-7
CHEBI:45223 ,
M0246
2-pyridyl mercaptan
1h-pyridine-2-thione
AKOS000120194
A837693
AKOS003596823
unii-ee982kt952
ee982kt952 ,
1,2-dihydropyridine-2-thione
2-mercapto pyridine
thiopyridone-2
A818409
einecs 249-657-7
pyridinethione
29468-20-0
c5h5ns
STL281380
alrithiol-2
FT-0612770
PS-6210
EPITOPE ID:120365
mercaptopyridine, 2-
SCHEMBL54576
AM81301
pridine-2-thiol
2-mercapto-pyridine
pyridin-2(1h)-thione
mercaptopyridine
pyridin-2-thiol
pyridine-2(1h)-thione
DTXSID9062568
F9995-0226
FT-0698903
J-524119
mfcd00006285
2-mercaptopyridine, vetec(tm) reagent grade, 98%
J-016402
SY009099
(2s,3s)-3-amino-2-methyl-4-oxo-1-azetidinesulfonicacid
i+/--thiopyridon
Q15274000
2-mercaptopyridine (thione form)
BCP21833
2637-34-5;2-pyridinethiol;pyridine-2-thiol;2-thiopyridine
2-pyridinethiol; 2-pyridinethione; 2-pyridyl mercaptan; 2-pyridylthiol; 2-sulfanylpyridine
2-thioxopyridine
thioxopyridine
A936845
EN300-21547
E81838
CS-0020126
PD007080
Z203045372
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
fluorescence quencherA compound used to return an excited fluorophore to the ground state by transfer of energy from fluorophore to quencher without the emission of light, with the quencher being promoted to its own excited state.
allergenA chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
[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 (2)

ClassDescription
pyridinesAny organonitrogen heterocyclic compound based on a pyridine skeleton and its substituted derivatives.
aryl thiolAn aryl thiol is a thiol in which a sulfanyl group, SH, is attached to an aryl group.
[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]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID584546Inhibition of inosine/L-alanine-induced Bacillus anthracis Sterne 34F2 spore germination pretreated for 15 mins before inosine/L-alanine challenge2010Antimicrobial agents and chemotherapy, Dec, Volume: 54, Issue:12
Testing nucleoside analogues as inhibitors of Bacillus anthracis spore germination in vitro and in macrophage cell culture.
AID584549Activation of Bacillus anthracis Sterne 34F2 spore germination after 1 hr2010Antimicrobial agents and chemotherapy, Dec, Volume: 54, Issue:12
Testing nucleoside analogues as inhibitors of Bacillus anthracis spore germination in vitro and in macrophage cell culture.
AID584550Cytotoxicity against mouse J774A1 cells2010Antimicrobial agents and chemotherapy, Dec, Volume: 54, Issue:12
Testing nucleoside analogues as inhibitors of Bacillus anthracis spore germination in vitro and in macrophage cell culture.
AID584547Antibacterial activity against Bacillus anthracis Sterne 34F2 infected in mouse J774A.1 cells assessed as protection against bacteria-induced cytotoxicity using propidium iodide staining after 3 hrs measured every hours for up to 7 hrs2010Antimicrobial agents and chemotherapy, Dec, Volume: 54, Issue:12
Testing nucleoside analogues as inhibitors of Bacillus anthracis spore germination in vitro and in macrophage cell culture.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (12.20)18.7374
1990's8 (19.51)18.2507
2000's10 (24.39)29.6817
2010's15 (36.59)24.3611
2020's3 (7.32)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.15

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

MetricThis Compound (vs All)
Research Demand Index30.15 (24.57)
Research Supply Index3.76 (2.92)
Research Growth Index4.75 (4.65)
Search Engine Demand Index33.89 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.15)

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%
Other42 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]