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Chemical compound
Quinoline is a heterocyclic aromatic organic compound with the chemical formula C9H7N. It is a colorless hygroscopic liquid with a strong odor. Aged samples
Quinoline
"Mixture of water-soluble organic compounds from Quinoline Yellow dye"
Quinoline Yellow WS (/ˈkwɪnəliːn/) is a mixture of organic compounds derived from the dye Quinoline Yellow SS (spirit soluble). Owing to the presence
Quinoline_Yellow_WS
Quinoline alkaloids are naturally occurring chemical compounds from the group of alkaloids, which are chemically derived from quinoline. Some quinoline
Quinoline_alkaloids
Chemical compound
Quinoline methiodide is a quaternary ammonium compound produced by reaction of quinoline with methyl iodide. It has paralyzing effects. Quaternary ammonium
Quinoline_methiodide
Topics referred to by the same term
Quinoline Yellow may refer to two chemically related dyes: Quinoline Yellow SS, a bright yellow dye Quinoline Yellow WS, a yellow food coloring It may
Quinoline_Yellow
Organic reaction
Combes quinoline synthesis is a chemical reaction, which was first reported by Combes in 1888. Further studies and reviews of the Combes quinoline synthesis
Combes_quinoline_synthesis
Fluorogenic amine labelling dye
3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde (CBQCA) is a fluorogenic amine labeling dye that is not fluorescent itself, but covalently reacts with
3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde
3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde
Fluorogenic amine labelling dye
3-(2-Furoyl)-quinoline-2-carboxaldehyde (FQ) is a fluorogenic amine labeling dye that is not fluorescent itself, but reacts with primary amines to form
3-(2-Furoyl)quinoline-2-carboxaldehyde
3-(2-Furoyl)quinoline-2-carboxaldehyde
Type of enzyme
In enzymology, quinoline 2-oxidoreductase (EC 1.3.99.17) is an enzyme that catalyzes the chemical reaction: Quinoline + electron acceptor H2O H2O
Quinoline_2-oxidoreductase
Chemical compound
(also known as oxine) is an organic compound derived from the heterocycle quinoline. A colorless solid, its conjugate base is a chelating agent, which is
8-Hydroxyquinoline
Chemical compound
isoquinoline" or isoquinolines. It is a structural isomer of quinoline. Isoquinoline and quinoline are benzopyridines, which are composed of a benzene ring
Isoquinoline
Chemical compound
Quinoline Yellow SS is a bright yellow dye with green shade. It is insoluble in water, but soluble in nonpolar organic solvents. Quinoline yellow is representative
Quinoline_Yellow_SS
Chemical reaction
The Niementowski quinoline synthesis is the chemical reaction of anthranilic acids and ketones (or aldehydes) to form γ-hydroxyquinoline derivatives.
Niementowski quinoline synthesis
Niementowski_quinoline_synthesis
Molecule with one or more rings composed of different elements
fused benzene derivatives of pyridine, thiophene, pyrrole, and furan are quinoline, benzothiophene, indole, and benzofuran, respectively. The fusion of two
Heterocyclic_compound
Organic synthesis reaction
The Camps quinoline synthesis (also known as the Camps cyclization) is a chemical reaction whereby an o-acylaminoacetophenone is transformed into two
Camps_quinoline_synthesis
Chemical reaction
β-unsaturated carbonyl compounds to form quinolines. This reaction is also known as the Skraup-Doebner-Von Miller quinoline synthesis, and is named after the
Doebner–Miller_reaction
Chemical compound
core chemical substructure of the aporphine alkaloids, a subclass of quinoline alkaloids. It can exist in either of two enantiomeric forms, (R)-aporphine
Aporphine
Chemical compound
Tetrahydroquinoline is an organic compound that is the semi-hydrogenated derivative of quinoline. It is a colorless oil. Substituted derivatives of tetrahydroquinoline
1,2,3,4-Tetrahydroquinoline
Species of flowering plant
gained the Royal Horticultural Society's Award of Garden Merit. Many quinoline alkaloids have been isolated from leaves of C. ternata. C. ternata contains
Choisya_ternata
Chemical compound
dyes, dubbed the "Southampton 6" (tartrazine, Allura Red, Ponceau 4R, Quinoline Yellow, sunset yellow, carmoisine), and sodium benzoate (a preservative)
Allura_Red_AC
Chemical reaction
synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives. It is named after German chemist Paul Friedländer (1857–1923)
Friedländer_synthesis
Class of pharmaceutical drugs
VEGFR-2 inhibitor, also known as kinase insert domain receptor(KDR) inhibitor, are tyrosine kinase receptor inhibitors that reduce angiogenesis or lymphangiogenesis
VEGFR-2_inhibitor
Medication used to treat malaria and babesiosis
alkaloid, a naturally occurring chemical compound. It possesses a C9H7N quinoline functional group (pyridine fused to benzene). Quinine was first isolated
Quinine
concentration, [ C l − ] {\displaystyle [Cl^{-}]} . in a linear manner. Thus, quinoline-based indicators are one-wavelength dyes - the signal results from monitoring
Fluorescent_chloride_sensor
Pharmaceutical compound
or as 6-methoxy-5-methyl-1,2,3,4,5-tetrahydropyrrolo[4,3,2-d,e]-quinoline, is a tricyclic cyclized tryptamine and analogue of 5-MeO-DMT and bufotenine
O-Methylnordehydrobufotenine
Chemical compound used as colorant
using six food additive colours, tartrazine, allura red, ponceau 4R, quinoline yellow WS, sunset yellow and carmoisine (dubbed the "Southampton 6") by
Sunset_yellow_FCF
Class of dyes
heteroaromatic moiety, such as pyrrole, imidazole, thiazole, pyridine, quinoline, indole, benzothiazole, etc. In addition, the polymethine chain of cyanines
Cyanine
In enzymology, quinoline-4-carboxylate 2-oxidoreductase (EC 1.3.99.19) is an enzyme that catalyzes the chemical reaction quinoline-4-carboxylic acid +
Quinoline-4-carboxylate 2-oxidoreductase
Quinoline-4-carboxylate_2-oxidoreductase
Chemical compound
of a mixture of six food dyes (tartrazine, Allura Red AC, ponceau 4R, Quinoline Yellow WS, sunset yellow and carmoisine, dubbed the "Southampton 6") and
Ponceau_4R
Pharmaceutical compound
3-(gamma-p-fluorobenzoyl propyl) 2,3,4,4a,5,6-hexahydro-1(H)-pyrazino(1,2-a) quinoline hydrochloride (compound 69-183, centpyraquin)". Experientia. 29 (12):
Centpyraquin
Catalyst enabling the hydrogenation of alkynes to alkenes
of other "catalyst poisons" have been used, including lead oxide and quinoline. The palladium content of the supported catalyst is usually 5% by weight
Lindlar_catalyst
Fluorogenic amine labelling dye
wavelength of 395 nm (deep violet, near UV). Fluorescamine 3-(2-Furoyl)quinoline-2-carboxaldehyde (FQ) "2,5-Dioxopyrrolidin-1-yl quinolin-6-ylcarbamate"
6-Aminoquinolyl-N-hydroxysuccinimidyl carbamate
6-Aminoquinolyl-N-hydroxysuccinimidyl_carbamate
Chemical compound
polypeptide is essential for the biosynthesis of the coenzyme pyrrolo-quinoline-quinone". J Bacteriol. 174 (4): 1426–7. doi:10.1128/jb.174.4.1426-1427
Pyrroloquinoline_quinone
Organic compound used in dyes
groups replaced by nitrogen. Like the related molecules pyridine and quinoline, acridine is mildly basic. It is an almost colorless solid, which crystallizes
Acridine
Chemical reaction used to synthesize quinolines
The Skraup synthesis is a chemical reaction used to synthesize quinolines. It is named after the Czech chemist Zdenko Hans Skraup (1850–1910). In the archetypal
Skraup_reaction
Chemical compound
two carboxylated quinoline rings. It is an organic compound with the formula (C9H5NCO2H)2. The molecule consists of a pair of quinoline rings, each bearing
Bicinchoninic_acid
Substance used to color food or drink
concentrations. Food colorants, synthetic Indigo carmine, blue Allura Red AC, red Quinoline Yellow WS, yellow Concerns over food safety led to numerous regulations
Food_coloring
Chemical compound
source of electrophilic bromine in halogenation reactions. The analogous quinoline compound behaves similarly. Pyridinium tribromide can be obtained by reacting
Pyridinium_perbromide
Class of naturally occurring chemical compounds
246 Hesse 2002, p. 58 Plemenkov 2001, p. 231 "Chemical Encyclopedia: Quinoline alkaloids". xumuk.ru. Aniszewski 2007, p. 114 Orekhov 1955, p. 205 Hesse
Alkaloid
Chemical reaction
Two systems exist for the asymmetric hydrogenation of 2-substituted quinolines with isolated yields generally greater than 80% and ee values generally
Asymmetric_hydrogenation
Pharmaceutical drug classification
ATC code P02 Anthelmintics is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed
ATC_code_P02
Chemical reaction
enamines. The reaction product in the original Povarov reaction is a quinoline. Because the reactions can be carried out with the three components premixed
Povarov_reaction
Chemical reaction
chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxylic acids. The reaction serves as an alternative to the Pfitzinger
Doebner_reaction
Chemical reaction
Limpach (1852–1933) in 1887 while they were studying the synthesis of quinoline derivatives. The mechanism begins with an attack of aniline on the keto
Conrad–Limpach_synthesis
Genus of flowering plants
ternata Choisya ternata Sundance = 'Lich' bred by Peter Catt (1986). Many quinoline alkaloids have been isolated from leaves of Choisya ternata. C. ternata
Choisya
Chemical compound
3-diazanaphthalene, quinazoline received its name from being an aza derivative of quinoline. Though the parent quinazoline molecule is rarely mentioned by itself
Quinazoline
Fluoroquinolone antibiotic
quinoline-3 ... – Google Patents". Wise R, Andrews JM, Edwards LJ (April 1983). "In vitro activity of Bay 09867, a new quinoline derivative
Ciprofloxacin
Chemical compound
Ethoxyquin (EMQ) is a quinoline-based antioxidant used as a food preservative in certain countries and originally to control scald on pears after harvest
Ethoxyquin
Class of antibacterial drugs, subgroup of quinolones
the fluoroquinolone class is based upon the quinoline ring system. Various substitutions made to the quinoline ring resulted in the development of numerous
Quinolone_antibiotic
Dessert originated in Germany
133) yellow colouring: sunset yellow FCF (E 110), Quinoline Yellow WS (E 104) green colouring: Quinoline Yellow WS (E 104), patent blue V (E 131), sunset
Götterspeise
Chemical compound
phenylhydroxylamine. It has been used as a mild oxidant in reactions like the Skraup quinoline synthesis. Nitrobenzene is toxic (Threshold Limit Value 5 mg/m3) and readily
Nitrobenzene
Chemical compound
formula C9H6NCH3. It is one of the two commercially important methyl quinolines. It is a colorless liquid, although impure samples can appear yellow.
Lepidine
Chemical compound
form of aminoquinoline with the amino group at the 4-position of the quinoline. The compound has been used as a precursor for the synthesis of its derivatives
4-Aminoquinoline
Chemical compound
good catalyst for the Skraup reaction for the synthesis of substituted quinolines. Bismuth phosphomolybdate catalyzes ammoxidation in the Sohio process
Phosphomolybdic_acid
Fluorogenic amine labelling dye
enabling an HPLC limit of detection of 10 fmol. Fluorescamine 3-(2-Furoyl)quinoline-2-carboxaldehyde (FQ) "4-Fluoro-7-nitrobenzofurazan". PubChem. National
4-Fluoro-7-nitrobenzofurazan
Book about isoquinoline alkaloids
The Simple Plant Isoquinolines is a 2002 book written by Alexander Shulgin and Wendy Perry about isoquinoline and tetrahydroisoquinoline alkaloids, for
The Simple Plant Isoquinolines
The_Simple_Plant_Isoquinolines
German chemist (1859–1921)
with Carl Paal, he discovered the Paal–Knorr synthesis, and the Knorr quinoline synthesis and Knorr pyrrole synthesis are also named after him. The synthesis
Ludwig_Knorr
Heterocyclic aromatic organic compound
Körner (1869) and James Dewar (1871) suggested that, in analogy between quinoline and naphthalene, the structure of pyridine is derived from benzene by
Pyridine
Polish chemist
– July 13, 1925 was a Polish chemist. He discovered the Niementowski quinoline synthesis and the Niementowski quinazoline synthesis. He was a president
Stefan_Niementowski
Chemical compound
4-Quinolone is an organic compound derived from quinoline. It and 2-quinolone are the two most important parent (meaning simplified) quinolones. 4-Quinolone
4-Quinolone
Chemical reaction
give the desired quinoline (5). Reaction of N-acyl isatins with base gives 2-hydroxy-quinoline-4-carboxylic acids. Camps quinoline synthesis Friedländer
Pfitzinger_reaction
Intravenous medication used in anesthesia
N-Methylstrychnine N,N-Dimethylmuscimol Nipecotic acid Pitrazepin Pseudostrychnine Quinolines (e.g., 4-hydroxyquinoline, 4-hydroxyquinoline-3-carboxylic acid, 5,7-CIQA
Propofol
Class of chemical compounds
6-hexahydrobenzo[f]quinoline-2-carboxamides and stereochemistry of diethyl 4-methyl-1-oxo-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline-2,2-dicarboxylate"
Partial_lysergamide
Chemical compound
4-Nitroquinoline 1-oxide (also known as 4-NQO, 4NQO, 4Nqo, NQO and NQNO) is a quinoline derivative and a tumorigenic compound used in the assessment of the efficacy
4-Nitroquinoline_1-oxide
Chemical compound
CH3C9H6N. It is one of the methyl derivatives of the heterocyclic compound quinoline. It is bioactive and is used in the preparation of various dyes. It is
Quinaldine
Antimalarial drug precursor
8-Aminoquinoline is the 8-amino derivative of quinoline. Often abbreviated AQ, it is a pale yellow solid. It is structurally analogous to 8-hydroxyquinoline
8-Aminoquinoline
German medicinal chemist (born 1934)
new cyclocondensation strategy using o-halo(aroyl) halides to access quinoline and azaquinoline carboxylic acids—an approach that became known as the
Klaus_Grohe
Pharmaceutical drug classification
ATC code G01 Gynecological antiinfectives and antiseptics is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system
ATC_code_G01
Organic compound (C6H5COOH)
borohydride. Decarboxylation to benzene may be effected by heating in quinoline in the presence of copper salts. Hunsdiecker decarboxylation can be achieved
Benzoic_acid
Syndrome of abnormally high activity
the "Southampton 6" (tartrazine, Allura Red AC (Red 40), Ponceau 4R, Quinoline Yellow, sunset yellow, carmoisine), and sodium benzoate (a preservative)
Hyperactivity
Chemical reaction
Gould–Jacobs reaction is an organic synthesis for the preparation of quinolines and 4‐hydroxyquinoline derivatives. The Gould–Jacobs reaction is a series
Gould–Jacobs_reaction
Chemical reaction
The Knorr quinoline synthesis is an intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using sulfuric acid. This reaction
Knorr_quinoline_synthesis
Pharmaceutical drug classification
Iodine/octylphenoxypolyglycolether Povidone-iodine# Diiodohydroxypropane Quinoline derivatives Dequalinium Chlorquinaldol Oxyquinoline Clioquinol Quaternary
ATC_code_D08
reaction is a series of chemical reactions that transforms quinoline to quinaldic acid.[1][2] Quinolines will react with acid chlorides and potassium cyanide
Reissert_reaction
Psychedelic drug
name (6aR,9R)-N,N-diethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide CAS Number 50-37-3 Y PubChem CID 5761 IUPHAR/BPS 17 DrugBank
LSD
Fluorogenic amine labelling dye
1674 Da to the target molecule. 3-(2-Furoyl)quinoline-2-carboxaldehyde (FQ) 3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde (CBQCA) Fluorescamine Wolfbeis
Pyrylium-1
Chemical compound
2-Quinolone is an organic compound related structurally to quinoline. It is the majority tautomer in equilibrium with 2-quinolinol. The compound can be
2-Quinolone
Yellow food coloring
effect of a mixture of six food dyes (Tartrazine, Allura Red, Ponceau 4R, Quinoline Yellow WS, Sunset Yellow and Carmoisine (dubbed the "Southampton 6"))
Tartrazine
Pharmaceutical compound
IUPAC name (6aR,9R)-N-butyl-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide CAS Number 50583-88-5 PubChem CID 3039392 ChemSpider 2302861
Lysergic_acid_butylamide
Chemical compound
BDBM50014407 2-(piperazin-1-yl)quinoline::2-Piperazin-1-yl-quinoline::2-Piperazin-1-yl-quinoline (Quipazine)::2-Piperazin-1-yl-quinoline(Quipazine)::CHEMBL18772::QUIPAZINE"
Quipazine
Chemical synthesis strategy
3-N-tosylaminophenol I with acrolein II affords a hydroxyl substituted quinoline III through 4 sequential steps without workup of the intermediate products
One-pot_synthesis
Chemical compound
structure and is also referred to as a quinoline or quinolinone SARM. LG121071 (LGD-121071), a tricyclic quinoline, was the predecessor compound of LGD-4033
LGD-4033
Class of drugs that hinder the action of leukotriene
receptor antagonists. Quinolines were shown to be good moiety for CysLT1 receptor antagonist. From weak antagonistic derivatives of quinolines, montelukast was
Cysteinyl-leukotriene type 1 receptor antagonists
Cysteinyl-leukotriene_type_1_receptor_antagonists
Chemical compound, antibiotic
PMID 7038329. US 4146719, Irikura T, "Piperazinyl derivatives of quinoline carboxylic acids", issued March 27, 1979, assigned to Kyorin Pharmaceutical
Norfloxacin
Medication used to treat malaria
the lysosomes of cells in the body.[citation needed] The pKa for the quinoline nitrogen of chloroquine is 8.5, meaning it is about 10% deprotonated at
Chloroquine
Species of flowering plant
alkaloids: Harmine 3-phenylquinoline, 3-(4-hydroxyphenyl)quinoline and 3-(1H-indol-3-yl)quinoline Peganum nigellastrum is stoloniferous and grows in patches
Peganum_nigellastrum
Organomercuric antiseptic for external use on minor cuts
Iodine/octylphenoxypolyglycolether Povidone-iodine# Diiodohydroxypropane Quinoline derivatives Dequalinium Chlorquinaldol Oxyquinoline Clioquinol Quaternary
Merbromin
Pharmaceutical compound
Catequentinib (INN; formerly anlotinib) is a pharmaceutical drug for the treatment of cancer. It is approved in China for the treatment of locally advanced
Catequentinib
Chemical compound
Dihydrosanguinarine is an alkaloid found in the herbs Corydalis adunca and Lamprocapnos spectabilis. It gets its name from the Sanguinaria canadensis plant
Dihydrosanguinarine
Chemical compound
starting material 5-methoxy-2-tetralone (1) into the octahydrobenzo[g]quinoline ring system with the correct stereochemistry required. This intermediate
Quinagolide
Chemical compound
The quinoline derivative diiodohydroxyquinoline (INN), or iodoquinol (USAN), brand name Diodoquin, can be used in the treatment of amoebiasis. It is poorly
Diiodohydroxyquinoline
mediocre yields. The Perkow reaction is also used in the synthesis of novel quinolines.[3] When the substituent is n-butyl the reaction product is the classical
Perkow_reaction
Naturally occurring combustible liquid
certain nitrogen heterocyclic compounds, such as pyridine, picoline, and quinoline are reported as contaminants associated with crude oil, as well as facilities
Petroleum
Pharmaceutical compound
9R)-N,N-diethyl-7-(2-phenylethyl)-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide PubChem CID 44457779 ChemSpider 23120272 ChEMBL ChEMBL23046
PHENETH-LAD
donor with other acceptors. The systematic name of this enzyme class is quinoline-2-carboxylate:acceptor 4-oxidoreductase (hydroxylating). This enzyme is
Quinaldate_4-oxidoreductase
reagent Cadiot–Chodkiewicz coupling Cadogan-Sundberg indole synthesis Camps quinoline synthesis Cannizzaro reaction Carbohydrate acetalisation Carbonyl reduction
List_of_organic_reactions
Pharmaceutical compound
lcarbamoyl]-8-methyl-N-propyl-4a,5,6,7,8a,9-hexahydro-4H-thieno[3,2-g]quinoline-6-carboxamide CAS Number 1399442-97-7 PubChem CID 66548529 DrugBank DB21715
Matsupexole
Method of separation in organic chemistry
fluid extraction Theoretical plate H. T. Clarke, Anne W. Davis (1922). "Quinoline". Organic Syntheses. 2: 79. doi:10.15227/orgsyn.002.0079. Fahlbusch, Karl-Georg;
Steam_distillation
Chemical compound
Quinclorac is an organic compound with the formula C9NH4Cl2CO2H. A colorless solid, it is soluble in hydrocarbons and alcohols. The compound is the carboxylic
Quinclorac
Rare and usually fatal brain infection by certain amoebae
"Functional Assessment of 2,177 U.S. and International Drugs Identifies the Quinoline Nitroxoline as a Potent Amoebicidal Agent against the Pathogen Balamuthia
Granulomatous amoebic encephalitis
Granulomatous_amoebic_encephalitis
QUINOLINE
QUINOLINE
QUINOLINE
QUINOLINE
Male
Native American
Native American Algonquin name ASKOOK means "snake."
Girl/Female
Australian, Irish
Bitter
Girl/Female
Tamil
Resurrection
Surname or Lastname
English
English : topographic name for someone who lived on a patch of land marked by an oak tree or trees, from Middle English oke ‘oak’ + land ‘land’.
Boy/Male
Tamil
Renounced, Illustrious
Girl/Female
American, Australian, British, Christian, English, French, German, Welsh
White; Fair; Blessed and Good; Fair and Good; Blessed; White Bro-wed; Moon; White Circle and Moon; Holy; Good
Male
Hindi/Indian
(कà¥à¤£à¤¾à¤²) Hindi name KUNAL means "lotus flower."
Boy/Male
English Irish Teutonic
Derivative of the Scandinavian god of battle 'Tyr.' Tuesday was named for Tyr.
Boy/Male
Hindu
To make Raj
Girl/Female
Hindu
Pious, Writing of the aryans
QUINOLINE
QUINOLINE
QUINOLINE
QUINOLINE
QUINOLINE
n.
A colorless liquid of a slightly pungent odor, C9H6N.CH3, first obtained as a condensation product of aldehyde and aniline, and regarded as a derivative of quinoline; -- called also methyl quinoline.
n.
A nitrogenous base C10H9N, extracted from coal-tar naphtha, as an oily liquid. It is a member of the quinoline series, and is probably identical with lepidine.
n.
One of the quinoline bases, obtained from coal tar as an oily liquid, C11H11N; also, any one of several substances metameric with, and resembling, cryptidine proper.
n.
A yellow, crystalline, organic dyestuff, C16H14N2, of artifical production. It is a strong base, and is a complex derivative of aniline and quinoline.
n.
An artificial alkaloid of the quinoline series, obtained as a white crystalline substance, C10H13NO, whose salts are valuable as antipyretics; -- so called from the green color produced in its solution by certain oxidizing agents.
n.
A nitrogenous organic base, C8H6N2, analogous to quinoline, obtained from certain complex diazo compounds.
n.
See Quinoline.
n.
A nitrogenous hydrocarbon base, C13H9N, analogous to phenanthrene and quinoline.
n.
One of a series of artificial blue or red dyes obtained from quinoline and lepidine and used in calico printing.
n.
A nitrogenous organic base from coal tar, and identical with quinoline. Cf. Quinoline.
n.
A white, crystalline, nitrogenous hydrocarbon, C9H9NO, obtained from certain derivatives of cinnamic acid and closely related to quinoline and carbostyril.
n.
An organic base obtained from quinoline. It is used as a febrifuge, and resembles kairine.
n.
One of several isomeric organic bases of the quinoline series of alkaloids.
n.
A pale buff or white crystalline alkaloid derived from quinoline, and used as an antipyretic in medicine.
n.
Hydroxy quinoline; a phenol derivative of quinoline, -- called also carbostyril.
n.
A nitrogenous base, C9H7N obtained as a pungent colorless liquid by the distillation of alkaloids, bones, coal tar, etc. It the nucleus of many organic bodies, especially of certain alkaloids and related substances; hence, by extension, any one of the series of alkaloidal bases of which quinoline proper is the type.