Page last updated: 2024-12-04

hydrogen cyanide

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Description

Hydrogen Cyanide: Hydrogen cyanide (HCN); A toxic liquid or colorless gas. It is found in the smoke of various tobacco products and released by combustion of nitrogen-containing organic materials. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hydrogen cyanide : A one-carbon compound consisting of a methine group triple bonded to a nitrogen atom [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 CID768
CHEMBL ID183419
CHEBI ID18407
MeSH IDM0010712

Synonyms (95)

Synonym
cyanwasserstoff
[chn]
methanenitrile
hydrogen(nitridocarbonate)
blausaeure
hydridonitridocarbon
CHEBI:18407 ,
caswell no. 483
un1613
aero liquid hcn
hydrogen cyanide, anhydrous, stabilized, absorbed in a porous inert material
evercyn
formic anammonide
blausaeure [german]
na1613
einecs 200-821-6
carbon hydride nitride (chn)
hydrogen cyanide, anhydrous, stabilized
ai3-31100-x
brn 1718793
hydrocyanic acid, anhydrous, stabilized, absorbed in a porous inert material
agent ac
cyanwasserstoff [german]
un1051
cyclon
hydrocyanic acid (prussic), unstabilized [forbidden]
cyjanowodor [polish]
zyklon b
hsdb 165
cyaanwaterstof [dutch]
rcra waste no. p063
prussic acid, anhydrous, stabilized, absorbed in a porous inert material
acide cyanhydrique [french]
hydrogen cyanide [iso]
acide cyanhydrique [iso-french]
rcra waste number p063
zaclondiscoids
un3294
prussic acid
epa pesticide chemical code 045801
cyclone b
un1614
hydrocyanic acid, anhydrous, stabilized
blauwzuur [dutch]
acido cianidrico [italian]
prussic acid, anhydrous, stabilized
un 1051
hydrocyanic acid
hydrogen cyanide
C01326
HCN ,
74-90-8
formonitrile
hydridonitridocarbonhydrogen(nitridocarbonate)methanenitrile
bdbm50152968
CHEMBL183419 ,
hydrogen cyanide, stabilized, with <3% water and absorbed in a porous inert material
hydrogen cyanide, stabilized with <3% water [un1051] [poison]
cyjanowodor
ec 200-821-6
ac [cyanide]
cyaanwaterstof
2wtb3v159f ,
hydrocyanic acid (prussic), unstabilized
hydrogen cyanide, stabilized with <3% water
hydrogen cyanide, stabilized, with <3% water and absorbed in a porous inert material [un1614] [poison]
acide cyanhydrique
acido cianidrico
unii-2wtb3v159f
blauwzuur
hydrogen cyanide [mi]
ac (chemical warfare agent)
hydrocyanicum acidum
hydrogen cyanide [hsdb]
hydrogen cyanide [who-dd]
hydrocyanicum acidum [hpus]
cyanide, hydrogen
blausaeure (german)
un 1614 (salt/mix)
nitrilomethane #
carbon hydride nitride
un 1613 (salt/mix)
zootic acid
prussic acid, unstabilized
na 1051
DTXSID9024148 ,
Q3416481
graphitic carbon nitride
143334-20-7
graphitic carbon nitride, 99%, length: 1 - 10 mum
carbon nitride (c3n4)
ac (cyanide)
acide cyanhydrique (iso-french)
dtxcid004148
(chn)

Research Excerpts

Overview

Hydrogen cyanide (HCN) is a small gaseous molecule that is predominantly produced as an equimolar co-product of ethylene (ET) biosynthesis in plants. It is a potent and fast-acting toxin increasingly recognized as an important cause of death in fire victims.

ExcerptReferenceRelevance
"Hydrogen cyanide (HCN) is a small gaseous molecule that is predominantly produced as an equimolar co-product of ethylene (ET) biosynthesis in plants. "( Comparative transcriptome analysis reveals significant differences in the regulation of gene expression between hydrogen cyanide- and ethylene-treated Arabidopsis thaliana.
Liu, Y; Xu, F; Yu, L, 2019
)
2.17
"Hydrogen cyanide (HCN) is a potent and fast-acting toxin increasingly recognized as an important cause of death in fire victims. "( Physiologically based pharmacokinetic modeling of hydrogen cyanide levels in human breath.
Johanson, G; Mörk, AK; Stamyr, K, 2015
)
2.11
"Hydrogen cyanide (HCN) is a secondary metabolite produced by many antagonistic Pseudomonas species. "( Hydrogen cyanide synthesis and antifungal activity of the biocontrol strain Pseudomonas fluorescens In5 from Greenland is highly dependent on growth medium.
Michelsen, CF; Stougaard, P, 2012
)
3.26
"Hydrogen cyanide (HCN) is a toxic chemical that can potentially cause mild to severe reactions in animals when grazing forage sorghum. "( Estimating hydrogen cyanide in forage sorghum ( Sorghum bicolor ) by near-infrared spectroscopy.
Fox, GP; Gleadow, RM; O'Donnell, NH; Stewart, PN, 2012
)
2.21
"Hydrogen cyanide (HCN) is a broad-spectrum antimicrobial compound involved in biological control of root diseases by many plant-associated fluorescent pseudomonads. "( Phylogeny of HCN synthase-encoding hcnBC genes in biocontrol fluorescent pseudomonads and its relationship with host plant species and HCN synthesis ability.
Défago, G; Frapolli, M; Moënne-Loccoz, Y; Ramette, A, 2003
)
1.76
"Hydrogen cyanide polymers are a plausible link between cosmochemistry and the origin of informational macromolecules."( Hydrogen cyanide polymers, comets and the origin of life.
Matthews, CN; Minard, RD, 2006
)
2.5

Effects

ExcerptReferenceRelevance
"Hydrogen cyanide (HCN) has been recognized as a potential biomarker for non-invasive diagnosis of Pseudomonas aeruginosa infection in the lung. "( Detection of hydrogen cyanide from oral anaerobes by cavity ring down spectroscopy.
Chen, W; Fogarty, CL; Groop, PH; Halonen, L; Lehto, M; Metsälä, M; Pussinen, PJ; Roslund, K, 2016
)
2.25

Toxicity

ExcerptReferenceRelevance
" This bench-scale method can simulate diverse fire conditions and identify extremely toxic smoke under both pre- and post-flashover conditions."( The development of a new small-scale smoke toxicity test method and its comparison with real-scale fire tests.
Levin, BC, 1992
)
0.28
"Methodology for the prediction of the toxic effects of fire effluents has made considerable progress [1,2]."( Modeling of toxicological effects of fire effluents: prediction of toxicity and evaluation of animal model.
Pauluhn, J, 1992
)
0.28
"The toxic effects of cassava diets on humans were reviewed."( The toxic effects of cassava (manihot esculenta grantz) diets on humans: a review.
Agunbiade, OO; Aregheore, EM, 1991
)
0.28
" DuPont's HCN experience has been combined with Aker Kvaerner's project engineering experience to insure the safe transfer of HCN technology to a licensee."( Assuring process safety in the transfer of hydrogen cyanide manufacturing technology.
Edwards, VH; Maxwell, GR; Robertson, M; Shah, K, 2007
)
0.6
" The present work aimed to evaluate the toxic effects of ingestion of cassava leaves by goats for 30 consecutive days, and to compare the results with the toxic effects of cyanide in goats, which have been described previously."( Toxic effects of prolonged administration of leaves of cassava (Manihot esculenta Crantz) to goats.
Górniak, SL; Soto-Blanco, B, 2010
)
0.36
" While harmonized testing guidelines and risk assessment paradigms are available for the quantification of thresholds for lethality or establishing no adverse effect levels, the quantification of 'impairment of escape' appears to be a more elusive goal."( Acute inhalation toxicity of carbon monoxide and hydrogen cyanide revisited: Comparison of models to disentangle the concentration × time conundrum of lethality and incapacitation.
Pauluhn, J, 2016
)
0.69
" Unfortunately, there is currently no foolproof method for determining the microbial consortium and providing a safe oral dosage for every patient."( Amygdalin: A Review on Its Characteristics, Antioxidant Potential, Gastrointestinal Microbiota Intervention, Anticancer Therapeutic and Mechanisms, Toxicity, and Encapsulation.
Abdellatif, AAH; Algheshairy, RM; Alhomaid, RM; Aljutaily, T; Almujaydil, MS; Almutairi, AS; Alshimali, SI; Barakat, H, 2022
)
0.72
" The interactions between QC and nanoparticles caused the nanocomposite pH-responsive behavior that assists in minimizing the side effect of the anticancer agent by controlling the burst release of QC at neutral conditions."( Development of chitosan/halloysite/graphitic‑carbon nitride nanovehicle for targeted delivery of quercetin to enhance its limitation in cancer therapy: An in vitro cytotoxicity against MCF-7 cells.
Khadiv-Parsi, P; Pourmadadi, M; Rashedi, H; Sabzini, M; Yazdian, F, 2023
)
0.91

Pharmacokinetics

ExcerptReferenceRelevance
" To explore this possibility, we developed a preliminary physiologically based pharmacokinetic model."( Physiologically based pharmacokinetic modeling of hydrogen cyanide levels in human breath.
Johanson, G; Mörk, AK; Stamyr, K, 2015
)
0.67
" The existing physiologically based pharmacokinetic (PBPK) model for HCN cannot clearly simulate continuous HCN inhalation or predict HCN levels in inhaled air."( Human continuous hydrogen cyanide inhalation predictor with a physiologically based pharmacokinetic (PBPK) model.
Lohitnavy, M; Phenrat, T; Tran, QB, 2020
)
0.9

Bioavailability

ExcerptReferenceRelevance
" The discussion is focused on toxic levels of hydrocyanate and oxalate, and the significance of the molar ratios in predicting the bioavailability of dietary zinc."( Hydrocyanate, oxalate, phytate, calcium and zinc in selected brands of Nigerian cocoa beverage.
Abara, AE; Aremu, CY, 1992
)
0.28
" The CHN biochemistry-based life would be applicable in habitats with a low bioavailability of oxygen, such as the alkane lakes of Titan and non-aquatic liquids on extrasolar bodies."( Oxygen-Free Biochemistry: The Putative CHN Foundation for Exotic Life in a Hydrocarbon World?
Li, YL; Lv, KP; Norman, L, 2017
)
0.46

Dosage Studied

ExcerptRelevanceReference
"Saskatoon serviceberry (Amelanchier alnifolia) twigs were administered to cattle in feed rations and by intraruminal dosing to determine the toxicity of the cyanogenic shrub."( Toxicity of Saskatoon serviceberry to cattle.
Clark, LJ; Majak, W; McLean, A; Udenberg, T, 1980
)
0.26
" This effect showed a clear dose-response relationship either with the amounts streamed or with the time during which sperm were exposed to cigarette smoke."( Use of a sealed minichamber for direct observation and evaluation of the in vitro effect of cigarette smoke on sperm motility.
Blumenfeld, Z; Brandes, JM; Makler, A; Reiss, J; Stoller, J, 1993
)
0.29
" The time-course and dose-response of ABA accumulation closely correlated with reductions in stomatal aperture and CO(2) assimilation and increased levels of hydrogen peroxide (H(2)O(2)), deoxyribonuclease (DNase) activity and chlorophyll loss."( Auxin herbicides induce H(2)O(2) overproduction and tissue damage in cleavers (Galium aparine L.).
Grossmann, K; Kwiatkowski, J; Tresch, S, 2001
)
0.31
" In phosgene, the signals of the 35Cl+ and 37Cl+ ions were clearly observed with high dose-response relationships in the parts-per-billion level, which could lead to the quantitative on-site analysis of CWAs."( Development of portable mass spectrometer with electron cyclotron resonance ion source for detection of chemical warfare agents in air.
Enomoto, S; Kidera, M; Kitagawa, M; Kondo, T; Sato, T; Seto, Y; Takahashi, K; Urabe, T, 2014
)
0.4
" Subsequently, the effects of pH value, photocatalyst dosage and MOX concentration on the photocatalytic behavior were also studied."( Aminobenzaldehyde convelently modified graphitic carbon nitride photocatalyst through Schiff base reaction: Regulating electronic structure and improving visible-light-driven photocatalytic activity for moxifloxacin degradation.
Bian, C; Dong, X; Li, Y; Liu, Y; Sun, P; Wang, W; Xiao, X; Xiao, Y, 2023
)
0.91
" Unfortunately, there is currently no foolproof method for determining the microbial consortium and providing a safe oral dosage for every patient."( Amygdalin: A Review on Its Characteristics, Antioxidant Potential, Gastrointestinal Microbiota Intervention, Anticancer Therapeutic and Mechanisms, Toxicity, and Encapsulation.
Abdellatif, AAH; Algheshairy, RM; Alhomaid, RM; Aljutaily, T; Almujaydil, MS; Almutairi, AS; Alshimali, SI; Barakat, H, 2022
)
0.72
" Moreover, the effects of chlorine time, chlorine dosage, pH, and CN dosage during the chlorination process were evaluated to understand the formation pattern of DBPs."( Effects of graphitic carbon nitride in the formation of disinfection byproducts.
Hu, J; Li, S; Lu, J; Mao, J; Ni, L; Wang, H, 2023
)
0.91
" By controlling the dosage of the europium modification, we can adjust the nitrogen defect content to reduce the energy gap and improve the CL performance."( Europium-Functionalized Graphitic Carbon Nitride for Efficient Chemiluminescence Detection of Singlet Oxygen.
Bai, Q; Gou, J; Liu, H; Xiao, X; Zhou, Y, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
poisonAny substance that causes disturbance to organisms by chemical reaction or other activity on the molecular scale, when a sufficient quantity is absorbed by the organism.
[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
hydracidA hydracid is a compound which contains hydrogen that is not bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
one-carbon compoundAn organic molecular entity containing a single carbon atom (C1).
[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 (92)

PathwayProteinsCompounds
Metabolism14961108
Metabolism of vitamins and cofactors146155
Metabolism of water-soluble vitamins and cofactors102114
Cobalamin (Cbl, vitamin B12) transport and metabolism1825
Amino acid and derivative metabolism250260
Sulfur amino acid metabolism2763
Degradation of cysteine and homocysteine1538
ethene biosynthesis I (plants)015
linustatin bioactivation010
superpathway of hydrolyzable tannin biosynthesis023
amygdalin and prunasin degradation09
thiosulfate disproportionation IV (rhodanese)15
dhurrin degradation36
lotaustralin degradation05
linamarin degradation210
ascorbate glutathione cycle518
cyanide degradation15
cornusiin E biosynthesis013
neolinustatin bioactivation07
taxiphyllin bioactivation05
ethylene biosynthesis I (plants)415
vicianin bioactivation113
cyanide detoxification I012
Methionine and Cysteine metabolism ( Methionine and Cysteine metabolism )2342
camalexin biosynthesis318
Cobalamin (Cbl) metabolism722
thiosulfate disproportionation III (rhodanese)15
nitrate reduction III (dissimilatory)1219
nitrate reduction VIII (dissimilatory)1915
formate to nitrite electron transfer714
nitrate reduction IX (dissimilatory)920
isopropanol biosynthesis (engineered)528
nitrate reduction V (assimilatory)426
superpathway of b heme biosynthesis from glycine1046
camalexin biosynthesis517
L-tryptophan degradation V (side chain pathway)020
L-tryptophan degradation I (via anthranilate)126
reductive acetyl coenzyme A pathway II (autotrophic methanogens)622
formate oxidation to CO2417
phenylacetate degradation II (anaerobic)015
D-galactarate degradation I530
superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation1855
pyruvate fermentation to acetone529
assimilatory sulfate reduction I1024
superpathway of Clostridium acetobutylicum solventogenic fermentation1444
superpathway of sulfate assimilation and cysteine biosynthesis1241
superpathway of microbial D-galacturonate and D-glucuronate degradation3592
L-asparagine degradation I425
thyroid hormone biosynthesis524
nitrite oxidation411
D-glucarate degradation I531
acetylene degradation121
amygdalin and prunasin degradation011
linamarin degradation215
superpathway of aromatic compound degradation via 2-hydroxypentadienoate5095
lotaustralin degradation18
neolinustatin bioactivation08
purine nucleobases degradation I (anaerobic)240
purine nucleobases degradation II (anaerobic)051
superpathway of aromatic compound degradation via 3-oxoadipate3681
m-cresol degradation116
2,5-xylenol and 3,5-xylenol degradation427
cyanide detoxification II15
L-tryptophan degradation VI (via tryptamine)319
ammonia oxidation IV (autotrophic ammonia oxidizers)724
ammonia oxidation I (aerobic)924
sulfide oxidation II (sulfide dehydrogenase)24
thioredoxin pathway28
fatty acid u03B1-oxidation I17
L-histidine degradation II522
L-histidine degradation VI120
L-valine biosynthesis1634
gluconeogenesis II (Methanobacterium thermoautotrophicum)1542
thiosulfate disproportionation IV (rhodanese)510
glycogen degradation I850
oxalate degradation III223
nitrogen fixation I (ferredoxin)619
Methanobacterium thermoautotrophicum biosynthetic metabolism2279
ascorbate glutathione cycle119
cyanide degradation012
cyanide detoxification I413
alkylnitronates degradation350
catechol degradation III (ortho-cleavage pathway)720
superpathway of bacteriochlorophyll a biosynthesis2270
tetrathionate reductiuon II (to trithionate)08
superpathway of D-glucarate and D-galactarate degradation637
cornusiin E biosynthesis014
superpathway of hydrolyzable tannin biosynthesis030
trans-4-hydroxy-L-proline degradation II643
tetrapyrrole biosynthesis II (from glycine)730
ethylene biosynthesis I (plants)815
methyl-coenzyme M oxidation to CO2017
methanogenesis from H2 and CO2322
methanogenesis from acetate526
formate to trimethylamine N-oxide electron transfer815
L-isoleucine biosynthesis II1430
L-isoleucine biosynthesis III019
nitrifier denitrification1425
chlorate reduction410
formate to dimethyl sulfoxide electron transfer914
nitrate reduction I (denitrification)719
Cysteine degradation619
Ethylene biosynthesis and signaling1116
Ethene biosynthesis from methionine114
Thiosulfate disproportionation III (rhodanese)13

Protein Targets (13)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carbonic anhydrase Stylophora pistillataKi580.00000.00000.686710.0000AID552130
Carbonic anhydraseStylophora pistillataKi860.00000.00000.50715.7100AID552131
Carbonic anhydrase 1Homo sapiens (human)Ki0.50000.00001.372610.0000AID1262263; AID1278739; AID1306523; AID238317; AID238513; AID238687; AID552127
Carbonic anhydrase 2Homo sapiens (human)Ki20.00000.00000.72369.9200AID1262264; AID1278740; AID1306524; AID238327; AID238542; AID238715; AID552128
Carbonic anhydrase 4Homo sapiens (human)Ki770.00000.00021.97209.9200AID238544
Carbonic anhydrase 6Homo sapiens (human)Ki70.00000.00011.47109.9200AID552129
Carbonic anhydrase 5A, mitochondrialHomo sapiens (human)Ki7.50000.00001.27259.9000AID238515; AID238688
Carbonic anhydraseMethanosarcina thermophilaKi680.00000.06000.97148.5000AID238607
Carbonic anhydrase 7Homo sapiens (human)Ki9,200.00000.00021.37379.9000AID265737
Carbonic anhydrase 9Homo sapiens (human)Ki4.00000.00010.78749.9000AID238546
Carbonic anhydraseMethanothermobacter thermautotrophicus str. Delta HKi27,800.00005.35005.35005.3500AID238958
Carbonic anhydrase 13Mus musculus (house mouse)Ki60.00000.00021.39749.9000AID238853
Carbonic anhydrase 5B, mitochondrialHomo sapiens (human)Ki7.50000.00001.34129.9700AID238515; AID238688
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (18)

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)
detection of chemical stimulus involved in sensory perception of bitter tasteCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 7Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 7Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 7Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 7Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 7Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 7Homo sapiens (human)
response to hypoxiaCarbonic anhydrase 9Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 9Homo sapiens (human)
response to xenobiotic stimulusCarbonic anhydrase 9Homo sapiens (human)
response to testosteroneCarbonic anhydrase 9Homo sapiens (human)
secretionCarbonic anhydrase 9Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 9Homo sapiens (human)
response to bacteriumCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (7)

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)
zinc ion bindingCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 7Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 7Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 9Homo sapiens (human)
protein bindingCarbonic anhydrase 9Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 9Homo sapiens (human)
molecular function activator activityCarbonic anhydrase 9Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (25)

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)
extracellular regionCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
cytosolCarbonic anhydrase 6Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytosolCarbonic anhydrase 7Homo sapiens (human)
cytoplasmCarbonic anhydrase 7Homo sapiens (human)
nucleolusCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
membraneCarbonic anhydrase 9Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 9Homo sapiens (human)
microvillus membraneCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (36)

Assay IDTitleYearJournalArticle
AID1306525Inhibition of Helicobacter pylori alpha carbonic anhydrase preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1262267Inhibition of Chionodraco hamatus alphaCA incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1306524Inhibition of human carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID265737Inhibition of human recombinant CA72006Bioorganic & medicinal chemistry letters, Jun-15, Volume: 16, Issue:12
Carbonic anhydrase inhibitors: inhibition of the cytosolic human isozyme VII with anions.
AID238515Inhibition constant of anion against human carbonic anhydrase isozyme hCA V2004Bioorganic & medicinal chemistry letters, Dec-06, Volume: 14, Issue:23
Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.
AID238513Inhibition constant of anion against human carbonic anhydrase isozyme hCA I2004Bioorganic & medicinal chemistry letters, Dec-06, Volume: 14, Issue:23
Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.
AID1306530Inhibition of Vibrio cholerae carbonic anhydrase beta preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1278741Inhibition of Vibrio cholerae alpha-carbonic anhydrase preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Mar-01, Volume: 26, Issue:5
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID1262263Inhibition of human CA1 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1306526Inhibition of Vibrio cholerae alpha carbonic anhydrase preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID552131Inhibition of Stylophora pistillata carbonic anhydrase 2 by stopped-flow CO2 hydration assay2011Bioorganic & medicinal chemistry letters, Jan-15, Volume: 21, Issue:2
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.
AID1306532Inhibition of Vibrio cholerae recombinant carbonic anhydrase gamma expressed in Escherichia coli DE3 cells preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID238688Inhibitory activity against human carbonic anhydrase V expressed in Escherichia coli2004Bioorganic & medicinal chemistry letters, Nov-01, Volume: 14, Issue:21
Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.
AID238853Inhibitory activity against mouse carbonic anhydrase XIII expressed in Escherichia coli TOP 102004Bioorganic & medicinal chemistry letters, Nov-01, Volume: 14, Issue:21
Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.
AID238542Inhibition constant of anion against human carbonic anhydrase isozyme hCA II2004Bioorganic & medicinal chemistry letters, Dec-06, Volume: 14, Issue:23
Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.
AID552127Inhibition of human recombinant CA1 by stopped-flow CO2 hydration assay2011Bioorganic & medicinal chemistry letters, Jan-15, Volume: 21, Issue:2
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.
AID238687Inhibitory activity against human carbonic anhydrase I expressed in Escherichia coli2004Bioorganic & medicinal chemistry letters, Nov-01, Volume: 14, Issue:21
Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.
AID238607Inhibitory constant against Zn-Cam (Methanosarcina thermophila)2004Bioorganic & medicinal chemistry letters, Sep-06, Volume: 14, Issue:17
Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.
AID238327Inhibitory constant against carbonic anhydrase II2004Bioorganic & medicinal chemistry letters, Sep-06, Volume: 14, Issue:17
Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.
AID1144175Drug excretion in po dosed beagle dog urine assessed as metabolite formation treated with [14C]-labelled N-Methyl-1,6-dihydropyridine-2-carbaldoxime hydrochloride by radiochromatography1976Journal of medicinal chemistry, Jan, Volume: 19, Issue:1
Improved delivery through biological membranes. 2. Distribution, excretion, and metabolism of N-methyl-1,6-dihydropyridine-2-carbaldoxime hydrochloride, a pro-drug of N-methylpyridinium-2-carbaldoxime chloride.
AID552130Inhibition of Stylophora pistillata carbonic anhydrase by stopped-flow CO2 hydration assay2011Bioorganic & medicinal chemistry letters, Jan-15, Volume: 21, Issue:2
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.
AID1278740Inhibition of human carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Mar-01, Volume: 26, Issue:5
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID1278742Inhibition of recombinant Vibrio cholerae beta-carbonic anhydrase expressed in competent Escherichia coli BL21(DE3) cells preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Mar-01, Volume: 26, Issue:5
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID552128Inhibition of human recombinant CA2 by stopped-flow CO2 hydration assay2011Bioorganic & medicinal chemistry letters, Jan-15, Volume: 21, Issue:2
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.
AID238317Inhibitory constant against carbonic anhydrase I2004Bioorganic & medicinal chemistry letters, Sep-06, Volume: 14, Issue:17
Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.
AID238653Inhibitory constant against carbonic anhydrase IV; nt= not tested2004Bioorganic & medicinal chemistry letters, Sep-06, Volume: 14, Issue:17
Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.
AID238544Inhibition constant of anion against human carbonic anhydrase isozyme hCA IV2004Bioorganic & medicinal chemistry letters, Dec-06, Volume: 14, Issue:23
Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.
AID1144179Retardation factor of the compound1976Journal of medicinal chemistry, Jan, Volume: 19, Issue:1
Improved delivery through biological membranes. 2. Distribution, excretion, and metabolism of N-methyl-1,6-dihydropyridine-2-carbaldoxime hydrochloride, a pro-drug of N-methylpyridinium-2-carbaldoxime chloride.
AID1278739Inhibition of human carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Mar-01, Volume: 26, Issue:5
Anion inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID238715Inhibitory activity against human carbonic anhydrase II expressed in Escherichia coli2004Bioorganic & medicinal chemistry letters, Nov-01, Volume: 14, Issue:21
Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.
AID552129Inhibition of human recombinant CA6 by stopped-flow CO2 hydration assay2011Bioorganic & medicinal chemistry letters, Jan-15, Volume: 21, Issue:2
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.
AID238546Inhibition constant of anion against human carbonic anhydrase isozyme hCA IX2004Bioorganic & medicinal chemistry letters, Dec-06, Volume: 14, Issue:23
Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.
AID238958Inhibitory constant against methanoarchaeon Methanobacterium thermoautotrophicum (Cab)2004Bioorganic & medicinal chemistry letters, Sep-06, Volume: 14, Issue:17
Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.
AID1306523Inhibition of human carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydrase assay2016Bioorganic & medicinal chemistry, 08-15, Volume: 24, Issue:16
Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID1262264Inhibition of human CA2 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (1,365)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990432 (31.65)18.7374
1990's137 (10.04)18.2507
2000's229 (16.78)29.6817
2010's301 (22.05)24.3611
2020's266 (19.49)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 89.06

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 Index89.06 (24.57)
Research Supply Index7.29 (2.92)
Research Growth Index4.76 (4.65)
Search Engine Demand Index163.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (89.06)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials5 (0.34%)5.53%
Reviews103 (7.03%)6.00%
Case Studies38 (2.59%)4.05%
Observational0 (0.00%)0.25%
Other1,320 (90.04%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]