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CUI2
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stringlengths
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C0000194
mapped_to
C3490344
2,2'-Dipyridyl
2-(6-fluoro-2,3'-bipyridin-5'-yl)-7-methyl-7-azabicyclo(2.2.1)heptane
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3490634
2,2'-Dipyridyl
4-(trans-2-methyl-2-butenoic acid)-2,2'-bipyridine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3493016
2,2'-Dipyridyl
1-(4-(5'-chloro-3,5-dimethyl-2,4'-bipyridin-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3493836
2,2'-Dipyridyl
Ni(cod)(bpy)
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3493999
2,2'-Dipyridyl
cerulomycin A
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3494000
2,2'-Dipyridyl
caerulomycin L
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3657197
2,2'-Dipyridyl
6,6'-bis(2-aminopyridyl)-2,2'-bipyridine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3659750
2,2'-Dipyridyl
3,3'-diamino-2,2'-bipyridine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3660170
2,2'-Dipyridyl
5,5'-dibromo-2,2'-bipyridine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3713121
2,2'-Dipyridyl
6,6'-bis(1,1-di(pyridin-2-yl)ethyl)-2,2'-bipyridine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C3884729
2,2'-Dipyridyl
SMY-540
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4079461
2,2'-Dipyridyl
bis(2,2'-bipyridine)(4,4'-ditridecyl-2,2'-bipyridine)ruthenium(II) dichloride
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4309554
2,2'-Dipyridyl
chloro(4-((2,2'-6',2'-terpyridin)-4'-yl)-N,N-diethylaniline)platinum(II)
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4309555
2,2'-Dipyridyl
dichloro(4-((2,2'-6',2'-terpyridin)-4'-yl)-N,N-diethylaniline)nickel(II)
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4506635
2,2'-Dipyridyl
D-607 compound
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4508725
2,2'-Dipyridyl
RAF709
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4548218
2,2'-Dipyridyl
5-((3,4'-bipyridin)-2'-yl)-N-(4-(pyrrolidin-1-ylmethyl)phenyl)-1,3,4-oxadiazol-2-amine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C4549668
2,2'-Dipyridyl
4'-terpyridinylsulfanylethylamine
A reagent used for the determination of iron.
null
C0000194
mapped_to
C5198269
2,2'-Dipyridyl
collismycin C
A reagent used for the determination of iron.
null
C0000194
mapped_to
C0175774
2,2'-Dipyridyl
Bipyridine
A reagent used for the determination of iron.
null
C0000204
mapped_to
C0069813
2,3-Diketogulonic Acid
oxyferriscorbone
Metabolite of ASCORBIC ACID and the oxidized form of the lactone DEHYDROASCORBIC ACID.
null
C0000215
inverse_isa
C0019236
2,4,5-Trichlorophenoxyacetic Acid
Herbicides
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.
C0000215
mapped_to
C0045424
2,4,5-Trichlorophenoxyacetic Acid
2,4,5-trichlorophenoxyethanol
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
mapped_to
C0074544
2,4,5-Trichlorophenoxyacetic Acid
fenoprop
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
mapped_to
C0604033
2,4,5-Trichlorophenoxyacetic Acid
4-(2,4,5-trichlorophenoxy)butyric acid
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
mapped_to
C0616425
2,4,5-Trichlorophenoxyacetic Acid
2,4,5-T propylene glycol butyl ester
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
mapped_to
C0620539
2,4,5-Trichlorophenoxyacetic Acid
2,4,5-T isooctyl ester
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
mapped_to
C0629567
2,4,5-Trichlorophenoxyacetic Acid
2,4,5-trichlorophenoxyacetic acid butyl ester
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
see_from
C0019236
2,4,5-Trichlorophenoxyacetic Acid
Herbicides
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.
C0000215
see_from
C0596330
2,4,5-Trichlorophenoxyacetic Acid
chlorophenoxyacetate
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
inverse_isa
C0019236
2,4,5-Trichlorophenoxyacetic Acid
Herbicides
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.
C0000215
isa
C0050961
2,4,5-Trichlorophenoxyacetic Acid
Agent Orange
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
A herbicide that contains equal parts of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), as well as traces of the contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin.
C0000215
isa
C1275576
2,4,5-Trichlorophenoxyacetic Acid
Agent Orange ll
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
isa
C1300582
2,4,5-Trichlorophenoxyacetic Acid
Agent Purple
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
inverse_isa
C0007066
2,4,5-Trichlorophenoxyacetic Acid
Carboxylic Acids
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
Organic compounds containing the carboxy group (-COOH). This group of compounds includes amino acids and fatty acids. Carboxylic acids can be saturated, unsaturated, or aromatic.
C0000215
inverse_isa
C0589321
2,4,5-Trichlorophenoxyacetic Acid
Phenoxyacid herbicide
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
replaced_by
C0303831
2,4,5-Trichlorophenoxyacetic Acid
2,3,5-Trichlorophenoxyacetic acid
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
has_causative_agent
C0416747
2,4,5-Trichlorophenoxyacetic Acid
Accidental poisoning by 2,4,5-T
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
has_causative_agent
C0589324
2,4,5-Trichlorophenoxyacetic Acid
Toxic effect of 2,4,5-trichlorophenoxyacetic acid
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
has_component
C2022268
2,4,5-Trichlorophenoxyacetic Acid
discharge testing soil sampling weed killers 2-4-5TP
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000215
has_causative_agent
C4074911
2,4,5-Trichlorophenoxyacetic Acid
Accidental poisoning caused by 2,4,5-Trichlorophenoxyacetic acid
An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed)
null
C0000220
inverse_isa
C0019236
2,4-Dichlorophenoxyacetic Acid
Herbicides
An herbicide with irritant effects on the eye and the gastrointestinal system.
Pesticides used to destroy unwanted vegetation, especially various types of weeds, grasses (POACEAE), and woody plants. Some plants develop HERBICIDE RESISTANCE.
C0000220
mapped_to
C0045455
2,4-Dichlorophenoxyacetic Acid
2,4-D amine
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0045456
2,4-Dichlorophenoxyacetic Acid
2,4-D n-butyl ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0045490
2,4-Dichlorophenoxyacetic Acid
2,4-dichlorophenoxyacetic acid isooctyl ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0045530
2,4-Dichlorophenoxyacetic Acid
4-(2,4-dichlorophenoxy)butyric acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0045665
2,4-Dichlorophenoxyacetic Acid
2-(2,4-dichlorophenoxy)ethylamine
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0054268
2,4-Dichlorophenoxyacetic Acid
butoxyethanol ester of 2,4-dichlorophenoxyacetic acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0057691
2,4-Dichlorophenoxyacetic Acid
dialen
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0057870
2,4-Dichlorophenoxyacetic Acid
dichlorprop
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0074025
2,4-Dichlorophenoxyacetic Acid
sangor
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0096864
2,4-Dichlorophenoxyacetic Acid
4-chlorophenoxyacetic acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0117446
2,4-Dichlorophenoxyacetic Acid
fenagon
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0529504
2,4-Dichlorophenoxyacetic Acid
dichlorprop methyl ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0602375
2,4-Dichlorophenoxyacetic Acid
NK 2 (2,4-dichlorophenoxy)acetic acid, (4-hydroxy-3-nitrophenyl)methyl ester)
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0612381
2,4-Dichlorophenoxyacetic Acid
2,4-dichlorophenoxyacetic acid propylene glycol butyl ether ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0614162
2,4-Dichlorophenoxyacetic Acid
2,5-dichloro-4-hydroxyphenoxyacetic acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0622863
2,4-Dichlorophenoxyacetic Acid
2-ethylhexyl 2,4-dichlorophenoxyacetate
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0626403
2,4-Dichlorophenoxyacetic Acid
dichlorprop-leucine conjugate
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0644016
2,4-Dichlorophenoxyacetic Acid
2-(2,4-dichlorophenoxy)propionic acid butoxyethyl ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0646926
2,4-Dichlorophenoxyacetic Acid
2,4-dichlorophenoxyacetic acid methyl ester
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
mapped_to
C0175776
2,4-Dichlorophenoxyacetic Acid
Dichlorophenoxyacetic acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
isa
C0050961
2,4-Dichlorophenoxyacetic Acid
Agent Orange
An herbicide with irritant effects on the eye and the gastrointestinal system.
A herbicide that contains equal parts of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), as well as traces of the contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin.
C0000220
isa
C1275576
2,4-Dichlorophenoxyacetic Acid
Agent Orange ll
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
isa
C1300582
2,4-Dichlorophenoxyacetic Acid
Agent Purple
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
inverse_isa
C0589321
2,4-Dichlorophenoxyacetic Acid
Phenoxyacid herbicide
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_causative_agent
C0275000
2,4-Dichlorophenoxyacetic Acid
2,4-Dichlorophenoxyacetic acid poisoning
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_causative_agent
C0416746
2,4-Dichlorophenoxyacetic Acid
Accidental poisoning by 2,4-D
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_component
C1266298
2,4-Dichlorophenoxyacetic Acid
2,4-Dichlorophenoxyacetate measurement
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_measured_component
C1266298
2,4-Dichlorophenoxyacetic Acid
2,4-Dichlorophenoxyacetate measurement
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_component
C2022054
2,4-Dichlorophenoxyacetic Acid
home drinking water sampling weed killers 2-4-D
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_component
C2022267
2,4-Dichlorophenoxyacetic Acid
discharge testing soil sampling weed killers 2-4-D
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000220
has_causative_agent
C4074870
2,4-Dichlorophenoxyacetic Acid
Accidental poisoning caused by 2,4-Dichlorophenoxyacetic acid
An herbicide with irritant effects on the eye and the gastrointestinal system.
null
C0000232
inverse_isa
C0021213
2,6-Dichloroindophenol
Indicators and Reagents
A dye used as a reagent in the determination of vitamin C.
Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant & Hackh's Chemical Dictionary, 5th ed, p301, p499)
C0000232
mapped_to
C0164388
2,6-Dichloroindophenol
2,6-dichloroindophenol oxidized
A dye used as a reagent in the determination of vitamin C.
null
C0000232
mapped_to
C0620345
2,6-Dichloroindophenol
2,3,6-trichloroindophenol
A dye used as a reagent in the determination of vitamin C.
null
C0000246
inverse_isa
C0014442
2-Acetolactate Mutase
Enzymes
An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate. EC 5.4.99.3.
Biological molecules that possess catalytic activity. They may occur naturally or be synthetically created. Enzymes are usually proteins, however CATALYTIC RNA and CATALYTIC DNA molecules have also been identified.
C0000246
inverse_isa
C0022202
2-Acetolactate Mutase
Isomerase
An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate. EC 5.4.99.3.
A class of enzymes that catalyze geometric or structural changes within a molecule to form a single product. The reactions do not involve a net change in the concentrations of compounds other than the substrate and the product.(from Dorland, 28th ed) EC 5.
C0000246
inverse_isa
C0033684
2-Acetolactate Mutase
Proteins
An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate. EC 5.4.99.3.
Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein.
C0000246
inverse_isa
C0524938
2-Acetolactate Mutase
Mutase
An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate. EC 5.4.99.3.
Enzymes of the isomerase class that catalyze the transfer of acyl-, phospho-, amino- or other groups from one position within a molecule to another. EC 5.4.
C0000246
disposition_of
C4521483
2-Acetolactate Mutase
Mutase (disposition)
An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate. EC 5.4.99.3.
null
C0000248
inverse_isa
C0007090
2-Acetylaminofluorene
Carcinogens
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included.
C0000248
mapped_to
C0045631
2-Acetylaminofluorene
2,7-bis((dipropylamino)acetamido)fluoren-9-one
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0045632
2-Acetylaminofluorene
2,7-bis((pyrrolidino)acetamido)fluoren-9-one
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0045633
2-Acetylaminofluorene
2,7-diacetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0045798
2-Acetylaminofluorene
2-acetylaminofluorene-N-sulfate
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0047191
2-Acetylaminofluorene
3-acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0047983
2-Acetylaminofluorene
4-acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0049888
2-Acetylaminofluorene
7-fluoro-N-2-acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0049917
2-Acetylaminofluorene
7-iodo-N-2-acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0067579
2-Acetylaminofluorene
N-(deoxyguanosin-8-yl)acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0067619
2-Acetylaminofluorene
N-acetoxy-7-ethyl-N-2-acetylaminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0068166
2-Acetylaminofluorene
N-myristoyloxy-N-acetyl-2-aminofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0068193
2-Acetylaminofluorene
N-nitroso-N(2)-fluorenylacetamide
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0609237
2-Acetylaminofluorene
2,7-bis((diethylamino)acetamido)fluoren-9-one
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0609238
2-Acetylaminofluorene
2,7-bis((morpholino)acetamido)fluoren-9-one
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0614567
2-Acetylaminofluorene
N-myristoyloxy-N-acetyl-2-amino-7-iodofluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0652829
2-Acetylaminofluorene
2-(bromoacetylamino)fluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0659038
2-Acetylaminofluorene
2-acetylaminofluoren-9-one
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null
C0000248
mapped_to
C0763933
2-Acetylaminofluorene
iodo-N-2-(4-hydroxyphenylacetamido)fluorene
A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.
null