Page last updated: 2024-12-05

thiocyanate

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Description

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

thiocyanate : A pseudohalide anion obtained by deprotonation of the thiol group of thiocyanic acid. [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 CID9322
CHEMBL ID127789
CHEBI ID18022
MeSH IDM0099575

Synonyms (41)

Synonym
thallium thiocyanate
nitridosulfidocarbonate(1-)
thiocyanate ion (1-)
ncs-
nitridothiocarbonate(1-)
CHEBI:18022
thiozyanat
nitridothiocarbonate(iv)
rhodanid
scn(-)
[s-c#n](-)
n#c-s(-)
302-04-5
thiocyanate anion
ammonium sulfocyanate
weedazol tl
scn-
thiocyanate ion
rhodanide
thiocyanate
thiocyanate ion (2-)
bdbm26983
scn(-1)
chembl127789
cyanosulfanide
NCGC00248651-01
NCGC00248651-02
71048-69-6
unii-o748su14om
o748su14om ,
ZMZDMBWJUHKJPS-UHFFFAOYSA-M
ZBKFYXZXZJPWNQ-UHFFFAOYSA-N
bdbm50098587
silver thiocyanate agscn
thiocyanid
DTXSID8047763
thiocyanic acid, ion(1-)
thiocyanate (ncs1-)
isothiocyanic acid, ion(1-)
Q60839
bdbm62293

Research Excerpts

Overview

Thiocyanate is a common pollutant in gold mine, textile, printing, dyeing, coking and other industries. It is an important molecule in the formation of biomolecules as well as a catalyst for prebiotic reactions. Thiocianate anion is a biomarker of exposure to tobacco smoke components which is characterized by a relatively long half-life in the human body.

ExcerptReferenceRelevance
"Thiocyanate is a common pollutant in gold mine, textile, printing, dyeing, coking and other industries. "( Treatment of thiocyanate-containing wastewater: a critical review of thiocyanate destruction in industrial effluents.
An, X; Lai, F; Li, N; Wang, L; Xiao, X; Xie, D; Zhang, Q, 2022
)
2.53
"Thiocyanate is an important molecule in the formation of biomolecules as well as a catalyst for prebiotic reactions."( Unexpected Thiocyanate Adsorption onto Ferrihydrite Under Prebiotic Chemistry Conditions.
de Carvalho Pereira, R; de Carvalho, PCG; Samulewski, RB; Zaia, CTBV; Zaia, DAM, 2020
)
1.67
"Thiocyanate anion is a biomarker of exposure to tobacco smoke components which is characterized by a relatively long half-life in the human body, i.e."( Determination of thiocyanate as a biomarker of tobacco smoke constituents in selected biological materials of human origin.
Jaszczak, E; Kiełbratowska, B; Kotłowska, A; Namieśnik, J; Narkowicz, S; Polkowska, Ż, 2018
)
1.54
"Thiocyanate is a heme peroxidase substrate that scavenges oxidants produced during inflammation and regulates host defense. "( Determination of thiocyanate in exhaled breath condensate.
Chandler, JD; Go, YM; Horati, H; Janssens, HM; Jones, DP; Pagliano, E; Scholte, BJ; Tirouvanziam, R; Veltman, M; Walker, DI, 2018
)
2.26
"The thiocyanate anion (SCN) is a normal component of the airway epithelial lining fluid (ELF) secreted by pulmonary epithelia with antioxidant and host defence functions."( Nebulized thiocyanate improves lung infection outcomes in mice.
Chandler, JD; Day, BJ; Huang, J; Min, E; Nichols, DP, 2013
)
1.27
"As thiocyanate (SCN(-)) acts as an important biomarker in human health assessment, there remains an urgent need to realize rapid and reproducible analysis of SCN(-) in body fluids. "( Rapid and reproducible analysis of thiocyanate in real human serum and saliva using a droplet SERS-microfluidic chip.
Cui, Y; Wang, Z; Wu, L; Zong, S, 2014
)
1.3
"Thiocyanate (SCN(-)) is a toxic contaminant produced by industrial processes such as gold ore cyanidation and coal coking. "( Thiocyanate adsorption on ferrihydrite and its fate during ferrihydrite transformation to hematite and goethite.
Moreau, JW; Vu, HP, 2015
)
3.3
"Thiocyanate (SCN(-)) is a small anion byproduct of cyanide metabolism. "( Ultrasensitive turn-on fluorescent detection of trace thiocyanate based on fluorescence resonance energy transfer.
Ma, LH; Song, J; Wan, YQ; Wu, FY, 2015
)
2.11
"Thiocyanate is a common contaminant of the gold mining and coal coking industries for which biological degradation generally represents the most viable approach to remediation. "( New insights into the genetic and metabolic diversity of thiocyanate-degrading microbial consortia.
Moreau, JW; Watts, MP, 2016
)
2.12
"Thiocyanate ion is a natural component of cow's milk (hereinafter as milk) which may be artificially augmented to activate the lactoperoxidase milk preservation system. "( Investigation of concentration of thiocyanate ion in raw cow's milk from China, New Zealand and the Netherlands.
Abernethy, G; Li, J; Liu, Z; Wang, Y; Yang, D; Yong, L, 2017
)
2.18
"Thiocyanate [SCN-] is a complex anion which is a potent inhibitor of iodide transport. "( Thiocyanate overload and thyroid disease.
Erdogan, MF, 2003
)
3.2
"Thiocyanate (SCN-) is a cyanide-related compound encountered in most POTW influents and may be decomposed to free cyanide (CN-) under some circumstances."( Effects of thiocyanate on the formation of free cyanide during chlorination and ultraviolet disinfection of publicly owned treatment works secondary effluent.
Dzombak, DA; Luthy, RG; Zheng, A,
)
1.24
"Thiocyanate is a chaotropic compound known to inhibit antigen-antibody binding in a concentration-dependent manner."( The relative affinity of recombinant dihydrolipoamide transacetylase for autoantibodies in primary biliary cirrhosis.
Coppel, RL; Dickson, ER; Fregeau, D; Gershwin, ME; Kaplan, M; Prindiville, T; Robertson, CA, 1990
)
1

Effects

Thiocyanate (SCN-) has concentration dependent antithyroid properties. A role in the etiology of goiter has been suggested in several studies.

ExcerptReferenceRelevance
"Thiocyanate (SCN-) has concentration dependent antithyroid properties and a role in the etiology of goiter has been suggested in several studies. "( The role of thiocyanate in the etiology of goiter in an industrial metropolitan area.
Below, H; Brauer, VF; Führer, D; Kramer, A; Paschke, R, 2006
)
2.16
"Thiocyanate ions, which have been proposed to enhance the antimicrobial activity of lysozyme, did not affect the antibacterial activity of HLZ or HLZ-HCO3- combinations."( Effects of lysozyme-thiocyanate combinations on the viability and lactic acid production of Streptococcus mutans and Streptococcus rattus.
Lumikari, M; Tenovuo, J, 1991
)
1.33

Actions

Thiocyanate (SCN-) plays a critical part in an oral antimicrobial system by acting as a substrate for peroxidases. The drug promotes inflammatory disease in rats and facilitates the anti-inflammatory action of historic metal therapies.

ExcerptReferenceRelevance
"Thiocyanate both (1) promotes inflammatory disease in rats and (2) facilitates the anti-inflammatory action of historic metal therapies based on gold (Au) or silver (Ag) in three models of chronic polyarthritis in rats."( Conditional pharmacology/toxicology V: ambivalent effects of thiocyanate upon the development and the inhibition of experimental arthritis in rats by aurothiomalate (Myocrysin®) and metallic silver.
Butters, D; Vernon-Roberts, B; Whitehouse, M, 2013
)
1.35
"Thiocyanate (SCN-) plays a critical part in an oral antimicrobial system by acting as a substrate for peroxidases. "( Inhibition by thiocyanate of muscarinic-induced cytosolic acidification and Ca2+ entry in rat sublingual acini.
Arreola, J; Melvin, JE; Zhang, GH, 1995
)
2.09
"Thiocyanate did not cause any difference on any cumulative concentration-response curves either on the vessels."( The effect of three products of cigarette smoke (cyanide, thiocyanate and nicotine) on the concentration-response curves of 5-hydroxytryptamine, norepinephrine and epinephrine in the isolated human umbilical veins and arteries.
Aydin, Y; Tikiz, H; Tunçel, N, 1994
)
1.25
"Thiocyanate did not inhibit TSH mediated cAMP production or Na+K+ ATPase activity, a sodium pump for iodide transport."( Examination of antithyroid effects of smoking products in cultured thyroid follicles: only thiocyanate is a potent antithyroid agent.
Fukayama, H; Murakami, S; Nasu, M; Sugawara, M, 1992
)
1.23

Toxicity

ExcerptReferenceRelevance
" Angiotensin-converting enzyme inhibitors are responsible for a plethora of adverse effects, including renal insufficiency, hypotension, angioedema, cough, and increased insulin sensitivity."( Toxic effects of drugs used in the ICU. Nitroprusside, nitroglycerin, and angiotensin-converting enzyme inhibitors.
Arnold-Capell, P; Curry, SC, 1991
)
0.28
" CHB is also a possible inducer of tissue glutathione in the liver and kidneys as well as in the pancreas, even at toxic doses."( Selective pancreato-toxicity in the rat induced by the naturally occurring plant nitrile 1-cyano-2-hydroxy-3-butene.
Fettman, MJ; Gould, DH; Wallig, MA, 1988
)
0.27
" Nitroprusside infusion, as described, in children with normal hepatic and renal function is safe and may not warrant routine assessment of thiocyanate levels."( Nitroprusside in children after cardiopulmonary bypass: a study of thiocyanate toxicity.
Cartmill, TB; Celermajer, JM; Kunathai, S; Nunn, GR; O'Halloran, M; Sholler, GF, 1989
)
0.71
" Analysis of cassava and its intermediate and final products for free cyanide, acetone cyanohydrin, and intact glucosides during the production of such cassava products as gari, fufu, and lafun revealed that while the finished products might be safe for human consumption, the workers were probably exposed at different stages of processing to nondietary sources of cyanide."( Cassava processing, consumption, and cyanide toxicity.
Adewusi, SR; Akindahunsi, AA, 1994
)
0.29
" The study indicates that (i) PCN was most toxic among all the cyanogens and (ii) beside cyanide, A-KG could be considered as an effective antidote for cyanogens."( Acute toxicity of some synthetic cyanogens in rats and their response to oral treatment with alpha-ketoglutarate.
Bhattacharya, R; Hariharakrishnan, J; Satpute, RM; Saxena, PB; Tripathi, H, 2009
)
0.35
" MCN was most toxic by oral (LD₅₀=66."( Acute toxicity of some synthetic cyanogens in rats: time-dependent cyanide generation and cytochrome oxidase inhibition in soft tissues after sub-lethal oral intoxication.
Bhattacharya, R; Gujar, NL; Rao, P; Singh, P; Yadav, SK, 2013
)
0.39

Pharmacokinetics

ExcerptReferenceRelevance
" After intravenous infusion, its serum half-life is about 15 minutes."( Clinical pharmacokinetics of nitroprusside, cyanide, thiosulphate and thiocyanate.
Schulz, V,
)
0.37

Bioavailability

ExcerptReferenceRelevance
" Drinking water samples from different sources were collected and iodine level was analysed to study the bioavailability of iodine in the region."( Iodine nutritional status of children in North East India.
Chandra, AK; Debnath, A; Khanam, J; Singh, LH; Tripathy, S, 2006
)
0.33
"Catalytic consumption of nitric oxide (NO) by myeloperoxidase and related peroxidases is implicated as playing a key role in impairing NO bioavailability during inflammatory conditions."( Mechanism and regulation of peroxidase-catalyzed nitric oxide consumption in physiological fluids: critical protective actions of ascorbate and thiocyanate.
Kettle, AJ; Maiocchi, SL; Rees, MD; Thomas, SR, 2014
)
0.6

Dosage Studied

Thiocyanate degradation and nitrification processes were actually inhibited by the free ammonia form ( NH3) in place of the ionized NH4 form (NH4+) Currently dosed and often unproperly named "ammonia" [IUPAC, 1997.

ExcerptRelevanceReference
"The urinary excretion of thiocyanate by hens after dosage with cyanide (30 mumol) has been studied in a series of acute experiments involving 6 hr urine collection periods."( Detoxication of cyanide in the chicken by conversion to thiocyanate, as influenced by the availability of transferable sulphur.
Davis, RH; Jalaludin, S; Oh, SY; Sykes, AH, 1987
)
0.82
" Fattening lambs got an analogous SCN- dosage with altogether 4 respectively 34 single doses under intensive keeping."( [Promotion of wool growth and body weight development of sheep by alimentary supplementation with thiocyanate].
Hiepe, T; Jülich, WD; Kramer, A; Thürkow, B; Völzke, M; Völzke, N; Weber, A; Weuffen, W,
)
0.35
" Thirty-four male goats were divided into five groups dosed with KCN at 0 (control)."( Physiopathological effects of the administration of chronic cyanide to growing goats--a model for ingestion of cyanogenic plants.
Górniak, SL; Kimura, ET; Soto-Blanco, B, 2001
)
0.31
" We explored the dose-response relationship of this association, using smoking history and serum cotinine and thiocyanate concentrations as measures of tobacco exposure."( Smoking history and serum cotinine and thiocyanate concentrations as determinants of rheumatoid factor in non-rheumatoid subjects.
Aho, K; Aromaa, A; Heliövaara, M; Knekt, P; Korpilähde, T; Marniemi, J, 2004
)
0.8
"The results are not in line with the hypothesis of a dose-response relationship between smoking exposure and RF positivity."( Smoking history and serum cotinine and thiocyanate concentrations as determinants of rheumatoid factor in non-rheumatoid subjects.
Aho, K; Aromaa, A; Heliövaara, M; Knekt, P; Korpilähde, T; Marniemi, J, 2004
)
0.59
"Extraction spectrophotometric method has been developed for the determination of tricyclic drugs such as trazodone (TZH), amineptine (APH) and amitriptyline (ATPH) hydrochlorides in pure form and in the dosage forms coming from different Egyptian markets."( Spectrophotometric determination of trazodone, amineptine and amitriptyline hydrochlorides through ion-pair formation with molybdenum and thiocyanate.
Khalil, SM; Mohamed, GG; Mohamed, NA; Nour El-Dien, FA, 2006
)
0.54
" Nevertheless, thiocyanate degradation and nitrification processes were actually inhibited by the free ammonia form (NH3) in place of the ionized NH4 form (NH4+) currently dosed and often unproperly named "ammonia" [IUPAC, 1997."( New approach to optimize operational conditions for the biological treatment of a high-strength thiocyanate and ammonium waste: pH as key factor.
Drakides, C; Lay-Son, M, 2008
)
0.92
" The effect of various parameters such as initial thiocyanate concentration, contact time, pH, particle size, resin dosage and temperature were studied."( Removal of thiocyanate from aqueous solutions by ion exchange.
Demirbas, E; Dizge, N; Kobya, M, 2009
)
1
"Three simple, accurate and sensitive methods (A-C) for the spectrophotometric assay of captopril (CPL) in bulk drug, in dosage forms and in the presence of its oxidative degradates have been described."( Utilization of oxidation reactions for the spectrophotometric determination of captopril using brominating agents.
El-Didamony, AM; Erfan, EA, 2010
)
0.36
" The proposed methods were applied for the determination of Ambroxol in tablet dosage forms."( Colorimetric and atomic absorption spectrometric determination of mucolytic drug ambroxol through ion-pair formation with iron and thiocyanate.
Levent, A; Sentürk, Z, 2010
)
0.57
"Three new, simple, sensitive, rapid and economical spectrophotometric methods (A, B and C) have been developed for the determination of propranolol hydrochloride (PRO) in bulk drug and dosage forms."( A sensitive spectrophotometric method for the determination of propranolol HCl based on oxidation bromination reactions.
El-Didamony, AM, 2010
)
0.36
"01) in a dose-response manner and active smoking was associated with lower adjusted levels of u-P8 (p<0."( Trends and variability in the levels of urinary thiocyanate, perchlorate, and nitrate by age, gender, race/ethnicity, smoking status, and exposure to environmental tobacco smoke over 2005-2012.
Jain, RB, 2016
)
0.69
" The developed PBPK model can be used in risk assessment to quantify dose-response effects of thiocyanate on TH."( Development of a PBPK model of thiocyanate in rats with an extrapolation to humans: A computational study to quantify the mechanism of action of thiocyanate kinetics in thyroid.
Lumen, A; Willemin, ME, 2016
)
0.94
" Further, we calculated both the mass balance of thiocyanate and the resultant plausible dosage of cyanide from the data reported in the previously published method."( Can excreted thiocyanate be used to detect cyanide exposure in live reef fish?
Andrade, L; Breen, NE; Loewenstein, J; Metivier, R; Rhyne, AL, 2018
)
1.1
" We tested the hypothesis of whether assuming a single mode of action of thyroidal iodide uptake inhibition is sufficient for describing the observed dose-response relationship for thiocyanate and its effects on serum thyroxine levels."( Characterization of the modes of action and dose-response relationship for thiocyanate on the thyroid hormone levels in rats using a computational approach.
Lumen, A; Willemin, ME, 2019
)
0.94
" Multivariate RCS logistic regression revealed a linear dose-response relationship between thiocyanate and elevated TG, TC, LDL-C, non-HDL-C, and Apo B, but a nonlinear relationship with lowered HDL-C (inflection point = 1."( Associations of thiocyanate, nitrate, and perchlorate exposure with dyslipidemia: a cross-sectional, population-based analysis.
Cheang, I; Gao, R; Guo, Q; Li, X; Liao, S; Shi, M; Zhu, Q; Zhu, X, 2023
)
1.48
" Thiocyanate also displayed a better dose-response than urinary cotinine."( Validation of Urinary Thiocyanate as a Robust Biomarker of Active Tobacco Smoking in the Prospective Urban and Rural Epidemiological Study.
Britz-McKibbin, P; Gill, B; Mathiaparanam, S; Paré, G; Sathish, T; Teo, KK; Yusuf, S, 2023
)
2.14
" In the adjusted models, for quartiles of PNT, statistically significant dose-response associations were observed in most relationships."( Environmental exposure to perchlorate, nitrate, and thiocyanate in relation to chronic kidney disease in the general US population, NHANES 2005-2016.
Li, W; Wu, H; Xu, X; Zhang, Y, 2023
)
1.16
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
[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
pseudohalide anion
sulfur molecular entity
[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]

Pathways (30)

PathwayProteinsCompounds
Metabolism14961108
Amino acid and derivative metabolism250260
Sulfur amino acid metabolism2763
Degradation of cysteine and homocysteine1538
Events associated with phagocytolytic activity of PMN cells213
Cysteine Metabolism923
beta-Mercaptolactate-Cysteine Disulfiduria923
Cystinosis, Ocular Nonnephropathic923
Sulfur Metabolism2833
Sulfur Metabolism (Butanesulfonate)2834
Sulfur Metabolism (Propanesulfonate)2834
Sulfur Metabolism (Ethanesulfonate)2834
Sulfur Metabolism (Isethionate)2834
Sulfur Metabolism (Methanesulfonate)2834
Thiosulfate Disproportionation III89
Immune System91482
Innate Immune System41475
ROS and RNS production in phagocytes1237
thiosulfate disproportionation IV (rhodanese)15
sulfur volatiles biosynthesis26
glucosinolate activation115
indole glucosinolate activation (herbivore attack)320
thiosulfate disproportionation III (rhodanese)15
glyceollin biosynthesis014
sulfur volatiles biosynthesis25
thyroid hormone biosynthesis524
thiocyanate degradation I04
thiocyanate degradation II411
fatty acid u03B2-oxidation I2316
thiosulfate disproportionation IV (rhodanese)510
superpathway of pterocarpan biosynthesis (via daidzein)026
indole glucosinolate activation (herbivore attack)424
Cysteine degradation619
Thiosulfate disproportionation III (rhodanese)13

Protein Targets (5)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carbonic anhydrase 1Homo sapiens (human)Ki8,202.02000.00001.372610.0000AID1798763; AID1803484
Carbonic anhydrase 2Homo sapiens (human)Ki8,482.02000.00000.72369.9200AID1798763; AID1803485
Carbonic anhydrase 4Homo sapiens (human)Ki10,202.52500.00021.97209.9200AID1798763
Carbonic anhydraseMethanosarcina thermophilaKi13,100.00000.06000.97148.5000AID1803493
Carbonic anhydrase 15Mus musculus (house mouse)Ki10,202.52500.00091.884610.0000AID1798763
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (13)

Processvia Protein(s)Taxonomy
one-carbon metabolic processCarbonic anhydrase 1Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 2Homo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 2Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 2Homo sapiens (human)
angiotensin-activated signaling pathwayCarbonic anhydrase 2Homo sapiens (human)
regulation of monoatomic anion transportCarbonic anhydrase 2Homo sapiens (human)
secretionCarbonic anhydrase 2Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 2Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 2Homo sapiens (human)
positive regulation of dipeptide transmembrane transportCarbonic anhydrase 2Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 2Homo sapiens (human)
carbon dioxide transportCarbonic anhydrase 2Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 2Homo sapiens (human)
bicarbonate transportCarbonic anhydrase 4Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (6)

Processvia Protein(s)Taxonomy
arylesterase activityCarbonic anhydrase 1Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 1Homo sapiens (human)
protein bindingCarbonic anhydrase 1Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 1Homo sapiens (human)
hydro-lyase activityCarbonic anhydrase 1Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 1Homo sapiens (human)
arylesterase activityCarbonic anhydrase 2Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 2Homo sapiens (human)
protein bindingCarbonic anhydrase 2Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 2Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 2Homo sapiens (human)
protein bindingCarbonic anhydrase 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 4Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (19)

Processvia Protein(s)Taxonomy
cytosolCarbonic anhydrase 1Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 1Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
cytosolCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
myelin sheathCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 2Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 4Homo sapiens (human)
rough endoplasmic reticulumCarbonic anhydrase 4Homo sapiens (human)
endoplasmic reticulum-Golgi intermediate compartmentCarbonic anhydrase 4Homo sapiens (human)
Golgi apparatusCarbonic anhydrase 4Homo sapiens (human)
trans-Golgi networkCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
external side of plasma membraneCarbonic anhydrase 4Homo sapiens (human)
cell surfaceCarbonic anhydrase 4Homo sapiens (human)
membraneCarbonic anhydrase 4Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 4Homo sapiens (human)
transport vesicle membraneCarbonic anhydrase 4Homo sapiens (human)
secretory granule membraneCarbonic anhydrase 4Homo sapiens (human)
brush border membraneCarbonic anhydrase 4Homo sapiens (human)
perinuclear region of cytoplasmCarbonic anhydrase 4Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (8)

Assay IDTitleYearJournalArticle
AID1798763CA Inhibition Assay from Article 10.1016/j.bmcl.2008.12.082: \\Carbonic anhydrase inhibitors: the membrane-associated isoform XV is highly inhibited by inorganic anions.\\2009Bioorganic & medicinal chemistry letters, Feb-15, Volume: 19, Issue:4
Carbonic anhydrase inhibitors: the membrane-associated isoform XV is highly inhibited by inorganic anions.
AID1803254CA Inhibition Assay from Article 10.3109/14756366.2011.649268: \\Inhibition of the alpha- and beta-carbonic anhydrases from the gastric pathogen Helycobacter pylori with anions.\\2013Journal of enzyme inhibition and medicinal chemistry, Apr, Volume: 28, Issue:2
Inhibition of the alpha- and beta-carbonic anhydrases from the gastric pathogen Helycobacter pylori with anions.
AID1803491ChEMBL_158311 (CHEMBL763368) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1803487ChEMBL_158307 (CHEMBL763192) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1803486ChEMBL_158306 (CHEMBL763191) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1803493ChEMBL_158313 (CHEMBL763370) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1803484ChEMBL_158304 (CHEMBL763189) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1803485ChEMBL_158305 (CHEMBL763190) from Article 10.1016/j.bmc.2016.05.029: \\Anion inhibition profiles of a-, u00DF- and u00BF-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.\\2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (1,174)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990399 (33.99)18.7374
1990's205 (17.46)18.2507
2000's255 (21.72)29.6817
2010's258 (21.98)24.3611
2020's57 (4.86)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 79.97

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 Index79.97 (24.57)
Research Supply Index7.15 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index143.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (79.97)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials37 (2.99%)5.53%
Reviews38 (3.07%)6.00%
Case Studies6 (0.49%)4.05%
Observational3 (0.24%)0.25%
Other1,153 (93.21%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]