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Chemical compound
Indole is an organic compound with the formula C6H4CCNH3. Indole is classified as an aromatic heterocycle. It has a bicyclic structure, consisting of a
Indole
Chemical compound
Indole-3-carbinol (I3C, C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous
Indole-3-carbinol
Class of alkaloids
Indole alkaloids are a class of alkaloids containing a structural moiety of indole; many indole alkaloids also include isoprene groups and are thus called
Indole_alkaloid
Biochemical method to identify bacteria
The indole test is a biochemical test performed on bacterial species to determine the ability of the organism to convert tryptophan into indole. This
Indole_test
Chemical compound
Indole-3-acetic acid (IAA, 3-IAA) is the most common naturally occurring plant hormone of the auxin class. It is the best known of the auxins, and has
Indole-3-acetic_acid
Chemical reaction
The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde
Fischer_indole_synthesis
Chemical compound
spelled skatol) or 3-methylindole is an organic compound belonging to the indole family. It occurs naturally in the feces of mammals and birds and is the
Skatole
Chemical compound
of indole-3-carbinol, found in cruciferous vegetables, such as broccoli, Brussels sprouts, cabbage and kale. It and its parent compound – indole-3-carbinol
3,3'-Diindolylmethane
Chemical compound
Indole-3-acetaldehyde (IAL) belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists
Indole-3-acetaldehyde
Class of enzymes
indole and glyceraldehyde-3-phosphate (G3P) from indole-3-glycerol phosphate (IGP). The β subunits catalyze the irreversible condensation of indole and
Tryptophan_synthase
Series of chemical reactions
The Reissert indole synthesis is a series of chemical reactions designed to synthesize indole or substituted-indoles (4 and 5) from ortho-nitrotoluene
Reissert_indole_synthesis
Chemical compound
5-b]indole is a tricyclic chemical compound related to tryptamine and having various alkaloid derivatives. The analogue of azepino[4,5-b]indole with
Azepino(4,5-b)indole
Canadian federal drug regulation act
1-pentyl-3-(1-naphthoyl)indole (JWH-018) 1-butyl-3-(1-naphthoyl)indole (JWH-073) 1-pentyl-3-(4-methyl-1-naphthoyl)indole (JWH-122) 1-hexyl-3-(1-naphthoyl)indole (JWH-019)
Controlled Drugs and Substances Act
Controlled_Drugs_and_Substances_Act
Chemical compound
Indole-3-butyric acid (1H-indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at
Indole-3-butyric_acid
Heteroannulation reaction
The Larock indole synthesis is a heteroannulation reaction that uses palladium as a catalyst to synthesize indoles from an ortho-iodoaniline and a disubstituted
Larock_indole_synthesis
Chemical reaction
The Bartoli indole synthesis (also called the Bartoli reaction) is the chemical reaction of ortho-substituted nitroarenes and nitrosoarenes with vinyl
Bartoli_indole_synthesis
Chemical compound
Indole-3-carbaldehyde (I3A), also known as indole-3-aldehyde and 3-formylindole, is a metabolite of dietary L-tryptophan which is synthesized by human
Indole-3-carbaldehyde
Chemical reaction
The Leimgruber–Batcho indole synthesis is a series of organic reactions that produce indoles from o-nitrotoluenes 1.[1][2][3] The first step is the formation
Leimgruber–Batcho indole synthesis
Leimgruber–Batcho_indole_synthesis
Chemical reaction
The Nenitzescu indole synthesis is a chemical reaction that forms 5-hydroxyindole derivatives from benzoquinone and β-aminocrotonic esters. This reaction
Nenitzescu_indole_synthesis
Index of chemical compounds with the same name
to: 1-(2-Aminopropyl)indole (1-API; 1-IT; α-methylisotryptamine; isoAMT; PAL-569) – an α-alkylisotryptamine 2-(2-Aminopropyl)indole (2-API; 2-IT) – neither
Aminopropylindole
The Gassman indole synthesis is a series of chemical reactions used to synthesize substituted indoles by addition of an aniline and a ketone bearing a
Gassman_indole_synthesis
Chemical compound
6-(2-Aminopropyl)indole (6-API, 6-IT) is an indole derivative which was first identified being sold on the designer drug market by a laboratory in the
6-(2-Aminopropyl)indole
Chemical compound
5-(2-Aminopropyl)indole (5-API or 5-IT), also known as 3,4-pyrrolo[b]amphetamine or by the code name PAL-571, is an indole and amphetamine derivative
5-(2-Aminopropyl)indole
Class of chemical compounds
Pyrrolidinylmethylindoles, or 3-(pyrrolidin-2-ylmethyl)-1H-indoles, also known as α,N-trimethylenetryptamines, are a group of cyclized tryptamines in
Pyrrolidinylmethylindole
Pharmaceutical compound
4-(2-Aminopropyl)indole (4-API), also known in the past as α-methylisotryptamine (α-Me-isoT), is a serotonin receptor modulator of the phenethylamine and
4-(2-Aminopropyl)indole
Chemical synthesis route
tryptamines like psilocin and 5-MeO-DiPT. It starts with indole or a ring-substituted indole. The scheme of the route is as follows: The route was first
Speeter–Anthony_route
Reagent used in microbiology
(DMAB) and thus can act as an indicator to presumptively identify indoles and urobilinogen. Several Ehrlich tests use the reagent in a medical test;
Ehrlich's_reagent
Chemical organic reaction
The Fukuyama indole synthesis is a versatile tin mediated chemical reaction that results in the formation of 2,3-disubstituted indoles. A practical one-pot
Fukuyama_indole_synthesis
Chemical reaction
can be heated in the presence of strong acid to produce an indole via the Fischer indole synthesis. If there is a leaving group elsewhere in the Japp–Klingemann
Japp–Klingemann_reaction
Reaction in organic chemistry
Cadogan–Sundberg indole synthesis, or simply Cadogan indole synthesis, is a name reaction in organic chemistry that allows for the generation of indoles from o-nitrostyrenes
Cadogan–Sundberg indole synthesis
Cadogan–Sundberg_indole_synthesis
Chemical compound
Kovac's reagent to test for indoles. The carbonyl group typically reacts with the electron rich 2-position of the indole but may also react at the C-3
Para-Dimethylaminobenzaldehyde
Para-Dimethylaminobenzaldehyde
Class of chemical compounds
analogue, also known as a substituted 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (or simply substituted hexahydroazepinoindole), is a derivative of noribogaminalog
Ibogalog
Species of bacterium
Proteus vulgaris is a rod-shaped, nitrate-reducing, indole-positive and catalase-positive, hydrogen sulfide-producing, Gram-negative bacterium that inhabits
Proteus_vulgaris
naphthylmethylindoles, naphthoylpyrroles, naphthylmethylindenes, indole-3-carboxamides, indole-3-carboxylates, indazole-3-carboxamides and sometimes others
Structural scheduling of synthetic cannabinoids
Structural_scheduling_of_synthetic_cannabinoids
Chemical compound
is a monoterpenoid indole alkaloid found in the leaves of Vinca minor (lesser periwinkle), comprising about 25–65% of its indole alkaloids by weight
Vincamine
Chemical compound
3-Indolepropionic acid (IPA), or indole-3-propionic acid, has been studied for its therapeutic value in the treatment of Alzheimer's disease. As of 2022
3-Indolepropionic_acid
indole-3-acetaldehyde oxidase (EC 1.2.3.7) is an enzyme that catalyzes the chemical reaction indole-3-acetaldehyde + H2O O2 H2O2 O2 H2O2 indole-3-acetic
Indole-3-acetaldehyde_oxidase
Chemical compound
reaction between indole-3-carboxaldehyde and nitropropane under amine salt or ionic liquid catalysis which produces 3-(2-nitrobut-1-enyl)-1H-indole,
Α-Ethyltryptamine
for the diagnostical indole test, to determine the ability of the organism to split indole from the amino acid tryptophan. The indole produced yields a red
Kovács_reagent
Microbiological and biochemical method for identification
action of enzyme tryptophanase is converted to an Indole molecule, pyruvate and ammonium. The indole is then extracted from the broth by means of xylene
IMViC
Chemical compound
10,11-Secoergoline, also known as 3-(2-piperidylmethyl)indole or as α,N-tetramethylenetryptamine, is the structure of ergoline in which the bond between
10,11-Secoergoline
Chemical compound
JWH-018 (1-pentyl-3-(1-naphthoyl)indole, NA-PIMO or AM-678) is an analgesic chemical from the naphthoylindole family that acts as a full agonist at both
JWH-018
Chemical compound
Dregamine is a naturally occurring monoterpene indole alkaloid found in several species in the genus Tabernaemontana including Ervatamia hirta and Tabernaemontana
Dregamine
Atypical opioid analgesic compound
7-Hydroxymitragynine (7-OH-MIT), often known simply in slang as 7-OH, is a terpenoid indole alkaloid present in the plant Mitragyna speciosa (the leaves of which are
7-Hydroxymitragynine
Pharmaceutical compound
N-dimethyltryptamine (DMT) in which the indole ring has been replaced with an indene ring. Put another way, the nitrogen atom in the indole ring of DMT has been replaced
C-DMT
Species of fungus
and 1.96% total indole content by dry weight. European fruiting bodies have been shown to have between 0.39% and 0.75% total indole content by dry weight
Psilocybe_cyanescens
Class of enzymes
Indole-3-pyruvate monooxygenase (EC 1.14.13.168, YUC2 (gene), spi1 (gene)) is an enzyme with systematic name indole-3-pyruvate,NADPH:oxygen oxidoreductase
Indole-3-pyruvate monooxygenase
Indole-3-pyruvate_monooxygenase
Pharmaceutical compound
also known as N,N-dimethylhomotryptamine or as 3-[3-(dimethylamino)propyl]indole, is a homotryptamine and homologue of the psychedelic tryptamine dimethyltryptamine
Dimethylhomotryptamine
Chemical reaction
The Hemetsberger indole synthesis (also called the Hemetsberger–Knittel synthesis) is a chemical reaction that thermally decomposes a 3-aryl-2-azido-propenoic
Hemetsberger_indole_synthesis
Pharmaceutical compound
N-pentamethylenetryptamine, N,N-piperidyltryptamine, or 3-(2-piperidinoethyl)indole, is a serotonin receptor modulator and possible serotonergic psychedelic
Pip-Tryptamine
Class of indoles
contain an indole ring system, joined to an amino (NH2) group via an ethyl (−CH2–CH2−) sidechain. In substituted tryptamines, the indole ring, sidechain
Substituted_tryptamine
Chemical compound
compound is based on the indole structure, but the 2-3 bond is saturated. By oxidation/dehydrogenation it can be converted to indole. Indoline can be produced
Indoline
Chemical compound
routes mainly via the Henry reaction aka Nitroadol condensation between indole-3-carboxaldehyde and nitroethane under amine salt or ionic liquid catalysis
Α-Methyltryptamine
Plant hormone
isolate one of these phytohormones and to determine its chemical structure as indole-3-acetic acid (IAA). Went and Thimann co-authored a book on plant hormones
Auxin
The Hegedus indole synthesis is a name reaction in organic chemistry that allows for the generation of indoles through palladium(II)-mediated oxidative
Hegedus_indole_synthesis
Indole 2,3-dioxygenase (EC 1.13.11.17) is an enzyme that catalyzes the chemical reaction[which?] indole O2 2-formylphenylformamide The two substrates
Indole_2,3-dioxygenase
Species of bacterium
K. pneumoniae, from which it is distinguished through its production of indole. This species was first described in 1886 when it was isolated from sour
Klebsiella_oxytoca
Pharmaceutical compound
analogue and bioisostere of 5-MeO-AMT in which the nitrogen atom of the indole ring has been replaced with an oxygen atom, resulting in the drug being
Mebfap
Species of plant
compounds in M. speciosa are indole alkaloids related to mitragynine, which is a tetracyclic relative of the pentacyclic indole alkaloids, yohimbine and voacangine
Mitragyna_speciosa
Chemical compound
AB-001 (1-pentyl-3-(1-adamantoyl)indole) is a designer drug that was found as an ingredient in synthetic cannabis smoking blends in Ireland in 2010 and
AB-001
Syntheses in organic chemistry
Baeyer–Emmerling indole synthesis is a method for synthesizing indole from a (substituted) ortho-nitrocinnamic acid and iron powder in strongly basic solution
Baeyer–Emmerling indole synthesis
Baeyer–Emmerling_indole_synthesis
Class of enzymes
Indole-3-acetate beta-glucosyltransferase (EC 2.4.1.121) is an enzyme that catalyzes the chemical reaction indole-3-acetic acid + UDP-glucose UDP
Indole-3-acetate beta-glucosyltransferase
Indole-3-acetate_beta-glucosyltransferase
Central nervous system stimulant
Amidephrine 2-Amino-1,2-dihydronaphthalene 2-Aminoindane 5-(2-Aminopropyl)indole 2-Aminotetralin Acridorex Amphetamine (Dextroamphetamine, Levoamphetamine)
Methamphetamine
Chemical compound
(1S)-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole Calligonine ((1R)-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole) Calligonine is a major alkaloid constituent
Tetrahydroharman
Chemical compound
Tryptophan is first deaminated to 3-indolepyruvate. It is then decarboxylated to indole acetaldehyde by indolepyruvate decarboxylase. This latter compound is transformed
Tryptophol
Pharmaceutical compound
psychedelic α-methyltryptamine (AMT) in which the benzene component of the indole ring has been removed. In contrast to tryptamines like AMT, 3-pyrrolylpropylamine
3-Pyrrolylpropylamine
Chemical compound
contains an α-amino group, an α-carboxylic acid group, and a side chain indole, making it a polar molecule with a non-polar aromatic beta carbon substituent
Tryptophan
Chemical compound
MPMI, also known as 3-(N-methylpyrrolidin-3-ylmethyl)indole or as N-methyl-α,N-trimethylenetryptamine, is a pyrrolidinylmethylindole and cyclized tryptamine
MPMI_(drug)
Class of enzymes
indole-3-acetaldehyde reductase (NADPH) (EC 1.1.1.191) is an enzyme that catalyzes the chemical reaction tryptophol + NADP+ H+ H+ indole-3-acetaldehyde
Indole-3-acetaldehyde reductase (NADPH)
Indole-3-acetaldehyde_reductase_(NADPH)
Chemical compound
is based on the indole structure, but in which a second benzene ring is fused onto the five-membered ring at the 2–3 position of indole (equivalent to
Carbazole
Chemical reaction
Bischler–Möhlau indole synthesis, also often referred to as the Bischler indole synthesis, is a chemical reaction that forms a 2-aryl-indole from an α-bromo-acetophenone
Bischler–Möhlau indole synthesis
Bischler–Möhlau_indole_synthesis
Chemical compound
potency and selectivity. Replacing the 3-(1-naphthoyl) group found in many indole derived cannabinoid ligands, with an adamantoyl group, generally confers
AM-1248
Psychedelic drug
hylamine::3-(2-dimethylaminoethyl)indole::3-[2-(dimethylamino)ethyl]indole::CHEMBL12420::DMT::N,N-dimethyl-1H-indole-3-ethylamine::N,N-dimethyltryptamine::US20240166618
Dimethyltryptamine
Chemical compound
APICA (2NE1, SDB-001, N-(1-adamantyl)-1-pentyl-1H-indole-3-carboxamide) is an indole based drug that acts as a potent agonist for the cannabinoid receptors
APICA (synthetic cannabinoid drug)
APICA_(synthetic_cannabinoid_drug)
Chemical compound
first of over 50 alkaloids that were discovered to share this type of bis-indole chemical structure. The chemical structure of staurosporine was elucidated
Staurosporine
Class of enzymes
Indole-2-monooxygenase (EC 1.14.14.153, BX2 (gene), CYP71C4 (gene)) is an enzyme with systematic name indole,NAD(P)H:oxygen oxidoreductase (2-hydroxylating)
Indole-2-monooxygenase
Species of bacterium
Proteus, P. hauseri is also able to convert tryptophan into indole, resulting in a positive indole test. P. hauseri shares a similar biochemical profile with
Proteus_hauseri
Chemical compound
on the synthesis and opioid agonistic activities of mitragynine-related indole alkaloids: discovery of opioid agonists structurally different from other
7-Acetoxymitragynine
Chemical compound
RCS-4, or 1-pentyl-3-(4-methoxybenzoyl)indole, is a synthetic cannabinoid drug sold under the names SR-19, BTM-4, or Eric-4 (later shortened to E-4), but
RCS-4
oxidoreductase (EC 1.2.7.8) is an enzyme that catalyzes the chemical reaction indole-3-pyruvic acid + coenzyme A + oxidised ferredoxin CO2 CO2 R=3-indoyl
Indolepyruvate ferredoxin oxidoreductase
Indolepyruvate_ferredoxin_oxidoreductase
Psychoactive drug, often called ecstasy
2016). "The new psychoactive substances 5-(2-aminopropyl)indole (5-IT) and 6-(2-aminopropyl)indole (6-IT) interact with monoamine transporters in brain tissue"
MDMA
Pharmaceutical compound
also known as N,N-tetramethylenetryptamine or as 3-(2-pyrrolidinoethyl)indole, is a lesser-known serotonin receptor modulator of the tryptamine and
Pyr-T
Pharmaceutical compound
5-HT2A receptor agonist and is described as a prodrug. It is a 3-pyrrolidine–indole derivative and hence cyclized tryptamine and is said to be psilocybin-like
MSP-2020
Chemical compound
Indolepropionamide (IPAM) is a chemical compound, an indole derivative with the molecular formula C11H12N2O. In vivo (rats), IPAM markedly reduced the
Indolepropionamide
Pharmaceutical compound
the nitrogen atom of the indole ring has been replaced with a sulfur atom, making the drug a benzothiophene rather than indole or tryptamine derivative
S-DMT
Species of legume
needed] Plant: Bufotenin and 5-MeO-DMT, DMT and its oxides, gramine, 15 indole-3-alkylamines, tryptophan bases, β-carbolines Seeds: Galactomannan, L-glucosyl
Phyllodium_pulchellum
Chemical compound
of indole. The term benzophosphole also refers to substituted derivatives of the parent heterocycle. Organophosphorus chemistry Phosphole Indole International
Benzophosphole
Enzyme
enzymology, indole-3-acetaldehyde reductase (NADH) (EC 1.1.1.190) is an enzyme that catalyzes the chemical reaction tryptophol + NAD+ H+ H+ indole-3-acetaldehyde
Indole-3-acetaldehyde reductase (NADH)
Indole-3-acetaldehyde_reductase_(NADH)
Enzyme that converts tryptophan into indole
chemical reaction L-tryptophan + H2O ⇌ {\displaystyle \rightleftharpoons } indole + pyruvate + NH3 This enzyme belongs to the family of lyases, specifically
Tryptophanase
Chemical compound
is an aromatic hydrocarbon. It is used in an acidic solution to detect indoles. The DMACA is any of a number of acidified DMACA solutions: 0.117 g of
P-Dimethylaminocinnamaldehyde
Class of chemical compounds
Pyrrolidinylethylindoles, or 3-(2-pyrrolidinylethyl)indoles, also known as pyr-tryptamines or N,N-tetramethylenetryptamines, are a group of cyclized tryptamines
Pyrrolidinylethylindole
Family of neurotransmitters
an indolamine is melatonin. In biochemistry, indolamines are substituted indole compounds that contain an amino group. Examples of indolamines include the
Indolamines
Species of bacterium
a Gram-negative, facultatively anaerobic, rod-shaped, nitrate-reducing, indole-negative bacterium. It shows swarming motility and urease activity. P. mirabilis
Proteus_mirabilis
Species of vine
Vietnamese and Thai incenses. A bast fibre is produced from the stems. Five indole alkaloids; coronaridine, voacangine, apparicine, conoflorine, and 19-epi-voacangarine
Trachelospermum_jasminoides
Class of enzymes
The enzyme indole-3-glycerol-phosphate synthase (IGPS) (EC 4.1.1.48) catalyzes the chemical reaction 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate
Indole-3-glycerol-phosphate synthase
Indole-3-glycerol-phosphate_synthase
Sulphide Indole Motility (SIM) medium is a bacterial growth medium which tests for the ability to reduce sulfates, the ability to produce indoles, and motility
Sulphide Indole Motility medium
Sulphide_Indole_Motility_medium
Biochemical reaction
The reaction relies on the interaction between glyoxylic acid and the indole ring of the amino acid tryptophan, a structural feature found in most proteins
Adamkiewicz_reaction
Chemical compound
Indole-5,6-quinone is an indolequinone, a chemical compound found in the oxidative browning reaction of fruits like bananas where it is mediated by the
Indole-5,6-quinone
Chemical compound
Secologanin then proceeds with dopamine or tryptamine to form ipecac and terpene indole alkaloids, respectively. Secologanin biosynthesis begins from geranyl pyrophosphate
Secologanin
Chemical compound
N-desmethylibogaminalog, also known as 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole, is a chemical compound and parent structure of the ibogalog group of compounds
Noribogaminalog
INDOLE
INDOLE
Surname or Lastname
English
English : nickname from Middle English loller ‘indolent fellow’, a derivative of lolle ‘to droop, dangle, or loll’.English : nickname from Middle English lollere ‘mumbler’, bestowed on a pious person or on a Lollard (a follower of the 14th-century religious reformer John Wyclif).
Surname or Lastname
English
English : nickname for an indolent person, from Middle English sleper ‘sleeper’.
Surname or Lastname
Welsh
Welsh : from the Welsh personal name Ith(a)el, Old Welsh Iudhail ‘bountiful lord’.English : habitational name from a place in West Yorkshire, which is probably named with a derivative of Old English īdel ‘unused ground’, ‘patch of waste land’.English : derogatory nickname from Middle English idel ‘idle’, ‘indolent’, ‘useless’, ‘worthless’, ‘devoid of good works’.
Surname or Lastname
English (chiefly West Country)
English (chiefly West Country) : nickname from Middle English chubbe ‘chub’, a common freshwater fish, Leuciscus cephalus. The fish is notable for its short, fat shape and sluggish habits. The word is well attested in Middle English as a description of an indolent, stupid, or physically awkward person, and this is probably the origin of modern English chubby, although the term has lost any pejorative overtones.
INDOLE
INDOLE
Boy/Male
Hindu, Indian, Tamil
Son of Lord Shiva and Parvati; Lord Ganesh
Girl/Female
Scottish
From the stream.
Boy/Male
Hindu, Indian
Calm; Shallow
Boy/Male
Muslim
A character in shahnameh
Female
Polish
Variant spelling of Polish Julita, JULITTA means "descended from Jupiter (Jove)."
Girl/Female
Australian, Hebrew
The Lord is Good
Girl/Female
Hindu, Indian, Marathi, Mythological, Sanskrit
Lord of Wealth
Female
Hungarian
Hungarian form of Roman Latin Victoria, VIKTÓRIA means "conqueror" or "victory."
Girl/Female
American, Australian, British, Christian, English, French, Hindu, Indian, Jamaican, Latin
Fruit; Cherry Fruit; Dear; Beloved; Form of Cheryl; Brotherly Love; Name of a Fruit; Darling; Cherry
Boy/Male
Hindu, Indian
Lose and Panni
INDOLE
INDOLE
INDOLE
INDOLE
INDOLE
n.
Indolence.
n.
An indolent, encysted tumor of the skin; especially, a sebaceous cyst.
n.
One who ate the fruit or leaf of the lotus, and, as a consequence, gave himself up to indolence and daydreams; one of the Lotophagi.
n.
Leisure; indolence; idleness; ease.
a.
Addicted to sloth; inactive; sluggish; lazy; indolent; idle.
n.
One who lives upon others; a pertinaceous and indolent dependent; a parasite; a sponger.
n.
Neglect of duty; idleness; indolence.
a.
To spend time lazily, whether lolling or idly sauntering; to pass time indolently; to stand, sit, or recline, in an indolent manner.
a.
Indulging in ease; avoiding labor and exertion; habitually idle; lazy; inactive; as, an indolent man.
a.
Causing little or no pain or annoyance; as, an indolent tumor.
v. t.
To bring to poverty; to impoverish; to ruin, as in reputation, morals, hopes, or the like; as, many are undone by unavoidable losses, but more undo themselves by vices and dissipation, or by indolence.
n.
An idle gait or stroll; the state of reclining indolently; a place of lounging.
n.
Listless indolence; dreaminess. Pope.
n.
The quality or condition of being indolent; inaction, or want of exertion of body or mind, proceeding from love of ease or aversion to toil; habitual idleness; indisposition to labor; laziness; sloth; inactivity.
v. i.
To act lazily or indolently; to recline; to lean; to throw one's self down; to lie at ease.
a.
Fat; indolent.
adv.
In an indolent manner.
v. t.
To yield to any influence, emotion, passion, or power; -- used reflexively; as, to surrender one's self to grief, to despair, to indolence, or to sleep.
a.
Negligent; heedless; indolent; listless.
v. i.
To be exited to thought or action from a state of indolence or inattention.