Search references for 5 HYDROXYINDOLINE. Phrases containing 5 HYDROXYINDOLINE
See searches and references containing 5 HYDROXYINDOLINE!5 HYDROXYINDOLINE
Chemical compound
5-Hydroxyindoline, also known as 2,3-dihydro-1H-indol-5-ol, is a psychoactive substance, saturated (hydrogenated) derivative of indole, which has a hydroxyl
5-Hydroxyindoline
Parkinson's medication
"Parcopa- Carbidopa and Levodopa tablet, orally disintegrating". DailyMed. 5 November 2007. Retrieved 15 August 2024. "Rytary- carbidopa and levodopa capsule
Carbidopa/levodopa
Dissociative hallucinogenic drug, mostly used recreationally
gait, slurred speech, bloodshot eyes, and loss of balance. Moderate doses (5–10 mg intranasal, or 0.01–0.02 mg/kg intramuscular or intravenous) will produce
Phencyclidine
Compound that activates dopamine receptors
cause the most side effects due to their lack of specificity, targeting D1, 5-HT and adrenergic receptors in addition to their intended D2 receptor target
Dopamine_agonist
Drug which blocks dopamine receptors
degenerative process". Reviews in the Neurosciences. 19 (4–5): 245–316. doi:10.1515/revneuro.2008.19.4-5.245. PMID 19145986. S2CID 29375454. Young SL, Taylor
Dopamine_antagonist
Chemical compound
of restless legs syndrome". Cochrane Database of Systematic Reviews. 2011 (5) CD005504. doi:10.1002/14651858.CD005504.pub2. PMC 8889887. PMID 21328278
L-DOPA
Class of pharmaceutical drugs
King MV, Marsden CA, Fone KC (September 2008). "A role for the 5-HT(1A), 5-HT4 and 5-HT6 receptors in learning and memory". Trends in Pharmacological
Atypical_antipsychotic
Peripheral D2 receptor antagonist
Gastroparesis. Elsevier. pp. 341–359. doi:10.1016/B978-0-12-818586-5.00025-9. ISBN 978-0-12-818586-5. S2CID 225132800. Worthington I, Pringsheim T, Gawel MJ, Gladstone
Domperidone
Amino acid
Nomenclature. 1983. Archived from the original on 9 October 2008. Retrieved 5 March 2018. "Tyrosine". The Columbia Electronic Encyclopedia, 6th ed. Infoplease
Tyrosine
Dopamine agonist medication
unaltered regardless of food presence. Steady-state is achieved within 3 days and 5 days for the IR and ER formulations, respectively. Pramipexole is eliminated
Pramipexole
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Alizapride
Antipsychotic medication
basis. It has actions at several 5-HT (serotonin) receptor subtypes. These are 5-HT2C, linked to weight gain, and 5-HT2A, linked to its antipsychotic
Risperidone
Wakefulness-promoting medication
levels of modafinil is typically 1.5 to 2.5 hours (range 1–4 hours). Food slightly slows the absorption of modafinil, by 0.5 to 1 hour, but does not affect
Modafinil
Species of plant
global public health action". Globalization and Health. 1 (5) 5. doi:10.1186/1744-8603-1-5. PMC 1143783. PMID 15847690. Table 2 Archived 2007-10-31 at
Salvia_divinorum
Class of drugs
haloperidol tends to block about 80% of D2 receptors at doses ranging from 2 to 5 mg per day. On the aggregate level, no typical antipsychotic is more effective
Typical_antipsychotic
Chemical compound
for the 5-HT4 receptors, unlike other benzamides such as cisapride and mosapride, which are 5-HT4 agonists. The affinity of cisapride for 5-HT4 receptors
Itopride
Atypical antipsychotic medication
like its parent compound risperidone, functions as an inverse agonist at 5-HT2A receptor 15. Paliperidone also acts as an antagonist of alpha-1 and alpha-2
Paliperidone
Dissociative anesthetic and anti-depressant
investigation. Blood or plasma ketamine concentrations are usually in a range of 0.5–5.0 mg/L in persons receiving the drug therapeutically (during general anesthesia)
Ketamine
Antipsychotic medication
the five known dopamine receptor subtypes (D1-4), but also block serotonin (5-HT2A, 2C), α1- and α2-adrenergic, and histamine H1 receptors. Compared to
Tiapride
Sedating antihistamine
antagonist (anticholinergic), and also has weak to moderate affinity for the 5-HT2A, 5-HT2C, D2, and α1-adrenergic receptors, where it acts as an antagonist
Promethazine
Dopaminergic medication
Journal of Medicine. 281 (5): 272. doi:10.1056/NEJM196907312810518. PMID 5791298. "Lasker Award". 1969. Archived from the original on 5 January 2016., retrieved
Levodopa
Antihypertensive agent
USP" (PDF). NDA 19-922/S-005. Archived from the original (PDF) on September 5, 2015. Nichols AJ, Ruffolo RR, Brooks DP (June 1990). "The pharmacology of
Fenoldopam
Typical antipsychotic medication
associated with extrapyramidal side effects. Doses of haloperidol greater than 5 mg increased the risk of side effects without improving efficacy. Patients
Haloperidol
Organic chemical that functions both as a hormone and a neurotransmitter
monoamines and acetylcholine". Pflügers Archiv. 447 (5): 636–40. doi:10.1007/s00424-003-1100-5. PMID 12827358. S2CID 20764857. Westerink RH (February
Dopamine
Isoquinoline alkaloid, found mainly in Corydalis
extracted an alkaloid from the root of Stephania rotunda with the yield of 1.2–1.5% and he named this compound rotundin. From 1950 to 1952, two Indian scientists
Tetrahydropalmatine
Atypical antipsychotic
antagonist at dopamine D2, D3 and to a lesser extent D4 receptors. Antagonism at 5-HT2A dominates in doses exceeding 600 mg daily. In doses of 600 to 1,600 mg
Sulpiride
Dopamine receptor agonist compound
several animal models, and is used to study its addiction effects to cocaine. 5-OH-DPAT 8-OH-DPAT PD-128,907 Rotigotine UH-232 "7-hydroxy-2-N,N-dipropylaminotetralin
7-OH-DPAT
Chemical compound
physiological effects of salvinorin A in humans. Conversely, the serotonin 5-HT2A receptor antagonist ketanserin was ineffective. Research has shown that
Salvinorin_A
Typical antipsychotic medication
nigrostriatal system produces the extrapyramidal effects Serotonin receptors (5-HT2, 5-HT6 and 5-HT7), with anxiolytic, antidepressant and antiaggressive properties
Chlorpromazine
Psychedelic drug
LSD may affect serotonin 5-HT1A, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT5A, and 5-HT6 receptors. Although not present in humans, serotonin 5-HT5B receptors found in
LSD
Dopamine receptor agonist compound
5-OH-DPAT is a synthetic compound that acts as a dopamine receptor agonist with selectivity for the D2 receptor and D3 receptor subtypes. Only the (S)-enantiomer
5-OH-DPAT
Dopamine receptor agonist compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
PF-592379
Chemical compound
A sequence of nine steps is required to transform the starting material 5-methoxy-2-tetralone (1) into the octahydrobenzo[g]quinoline ring system with
Quinagolide
Tricyclic antidepressant
1986). "Pharmacological differentiation and characterization of 5-HT1A, 5-HT1B, and 5-HT1C binding sites in rat frontal cortex". Journal of Neurochemistry
Amitriptyline
Chemical compound
contrast to metoclopramide, metopimazine does not interact with serotonin 5-HT3 and 5-HT4 receptors. Metopimazine is an approved prescription drug in France
Metopimazine
Atypical antipsychotic medicine
receptor. It is a partial agonist at the serotonin 5-HT1A receptor and acts as an antagonist at 5-HT2B and 5-HT2A receptors. It is taken by mouth. The most
Cariprazine
Class of chemical compounds
(lysergamides), and ergopeptides, with [LSD] belonging to the ergoamide class. 2.5 Lysergic acid and LSD, page 6970 Wong G, Lim LR, Tan YQ, Go MK, Bell DJ, Freemont
Lysergamides
Antipsychotic medication
administration in the 36 dogs that received the drug, and the seizures abated for 1.5 to 8 hours (n=6) or did not recur (n=2) in eight of 10 dogs that were actively
Acepromazine
Investigational dopamine antagonist
receptor antagonist. It shows little affinity for either dopamine D2-like or 5-HT2 receptors. Based on its profile in animal models, ecopipam was first studied
Ecopipam
Typical antipsychotic medication
Oral fluphenazine rapidly absorbs and plasma levels peak at about 1.0-2.5 ng/mL 2 hours post-ingestion. The volume of distribution is about 298 L due
Fluphenazine
Chemical compound
dopamine receptors (DRD1, DRD2, DRD4) as well as of 5-HT2A, 5-HT2C receptors, mAChRs (1 through 5), α1 adrenergic receptor and H1 receptor. Thiethylperazine
Thiethylperazine
Antihistamine drug
related to dyskinesia have also anecdotally been reported after periods of 7.5 months, such as continual head rolling, lip licking, and other forms of athetoid
Hydroxyzine
Typical antipsychotic medication
027 nM) and D4 (Ki 0.066 nM)) with weaker serotonin receptor antagonism (5-HT2A (Ki 3.75 nM)). In high doses, it has antihistaminergic and alpha-adrenergic[which
Benperidol
Antipsychotic medication
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Remoxipride
Antipsychotic medication
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Sultopride
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Rolicyclidine
Type of medication
potentiates the central effects of L-DOPA by decreasing the dose-dependency 4-5 fold, therein allowing for effective Parkinson's disease treatment without
Aromatic L-amino acid decarboxylase inhibitor
Aromatic_L-amino_acid_decarboxylase_inhibitor
Medication
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Eticyclidine
Chemical compound
extract from Piper methysticum Forster (kava-kava)". Pharmacopsychiatry. 31 (5): 187–192. doi:10.1055/s-2007-979325. PMID 9832350. S2CID 25270815. Baum,
Desmethoxyyangonin
Atypical antipsychotic
adjunctive therapy with an oral antidepressant. The most common adverse effects (≥5%) were somnolence and dry mouth. Lumateperone is associated with a low rate
Lumateperone
involves partial agonism at postsynaptic serotonin 5-HT1A receptors and full agonism at presynaptic 5-HT1A autoreceptors, which initially reduces serotonergic
Buspirone
Main receptor for most antipsychotic drugs
cytoplasmic half of the structure, particularly at the transmembrane domains (TM) 5 and 6. The conformational transitions occurred at the cytoplasmic ends are
Dopamine_receptor_D2
Atypical antipsychotic medication
Serotonin 5-HT1A receptor partial agonist, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT3, 5-HT6, and 5-HT7 receptor antagonist, and 5-HT1B, 5-HT1D, 5-HT1E, and 5-HT1F receptor
Quetiapine
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Quinpirole
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Tavapadon
Antiemetic medication
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Trimethobenzamide
Type of α-amino acid
Nomenclature. 1983. Archived from the original on 9 October 2008. Retrieved 5 March 2018. "IUPAC-IUB Commission on Biochemical Nomenclature A One-Letter
Phenylalanine
Hormone used as a medication
International Union of Basic and Clinical Pharmacology. Archived from the original on 5 February 2016. Retrieved 29 January 2016. "Neoatricon EPAR". European Medicines
Dopamine_(medication)
Medication for nausea, psychosis, and anxiety
[104-16-5] (2) in the presence of sodamide gives Prochlorperazine (3); or by alkylation of 2-Chloro-10-(3-chloropropyl)phenothiazine [2765-59-5] (4) and
Prochlorperazine
Chemical compound
nausea and vomiting of pregnancy". J Bras Ginecol (in Portuguese). 91 (4): 283–5. "Bula do Profissional de Saúde: Bromoprida". Bulário Eletrônico da Anvisa
Bromopride
Sedating antidepressant
receptor Strong: α1-adrenergic receptor, 5-HT2A and muscarinic acetylcholine receptors Moderate: 5-HT2C and 5-HT1A receptors Weak: α2-adrenergic and D2
Doxepin
Medication
8 nM), where it is a receptor antagonist, and is also a mixed 5-HT3 receptor antagonist/5-HT4 receptor agonist. The antiemetic action of metoclopramide
Metoclopramide
yl)-2β-(3'-phenylisoxazol-5'-yl)nortropane (FE-β-CPPIT) • N-(3'-Fluoropropyl-)-3β-(4'-chlorophenyl)-2β-(3'-phenylisoxazol-5'-yl)nortropane (FP-β-CPPIT) •
List_of_dopaminergic_drugs
Subfamily of dopamine receptors
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
D1-like_receptor
Chemical compound
Drug-Drug Interaction Risk Profile". Journal of Medicinal Chemistry. 65 (5): 3786–3797. doi:10.1021/acs.jmedchem.1c01887. PMID 35175768. S2CID 246942987
Mevidalen
D1 receptor positive allosteric modulator under development for Parkinson's disease
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Glovadalen
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
1-Methyl-3-propyl-4-(p-chlorophenyl)piperidine
1-Methyl-3-propyl-4-(p-chlorophenyl)piperidine
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Razpipadon
Substance related to dopamine functions
Arch Psychiatry Clin Neurosci. 255 (3): 190–201. doi:10.1007/s00406-005-0587-5. PMID 15995903. Curran MP, Perry CM (2002). "Spotlight on amisulpride in schizophrenia"
Dopaminergic
Experimental antidepressant drug
Conversely, ENX-104 showed little or no functional activity at the serotonin 5-HT1A or 5-HT7 receptor. ENX-104 is a benzamide derivative. It is a partially-deuterated
ENX-104
Atypical antipsychotic medication
gradually increased over a number of weeks. Initial doses may range from 6.5 to 12.5 mg/d, increasing stepwise typically, to doses in the range of 250–350 mg
Clozapine
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Pukateine
Class of G protein-coupled receptors
D4. D1-2 receptor subtypes are found at 10–100 times the levels of the D3-5 subtypes. The D1-like family receptors are coupled to the G protein Gsα. D1
Dopamine_receptor
Class of medications
many TCAs also have high affinity as antagonists at the 5-HT1, 5-HT2 (5-HT2A and 5-HT2C), 5-HT6, 5-HT7, α1-adrenergic, and NMDA receptors, and as agonists
Tricyclic_antidepressant
Atypical antipsychotic medication
as a partial agonist at dopamine D3 and D4 receptors and at serotonin 5-HT1A and 5-HT2C receptors. It is a third-generation antipsychotic and its introduction
Aripiprazole
Chemical compound
Biomedical and Life Sciences. 773 (1): 25–33. doi:10.1016/S1570-0232(01)00578-5. PMID 12015267. Springer D, Paul LD, Staack RF, Kraemer T, Maurer HH (August
4'-Methyl-α-pyrrolidinopropiophenone
4'-Methyl-α-pyrrolidinopropiophenone
Chemical compound
overall activity. The 3R,4S enantiomer demonstrates the highest selectivity for 5-HTT. In animal studies, DMNPC exhibits similar potency as fluoxetine, but
N,O-Dimethyl-4-(2-naphthyl)piperidine-3-carboxylate
N,O-Dimethyl-4-(2-naphthyl)piperidine-3-carboxylate
Pharmaceutical compound
LEK-8842. The drug shows affinity for serotonin 5-HT2 and α1-adrenergic receptors (Ki = 16.3 nM at 5-HT2) and acts as a silent antagonist of these receptors
LEK-8841
Antidepressant
α1-adrenergic receptor, the histamine H1 receptor, the serotonin 5-HT2A, 5-HT2C, 5-HT3, 5-HT6, and 5-HT7 receptors, the dopamine D1, D2, and D3 receptors, and
Clomipramine
Chemical compound
serotonin 5-HT1A, 5-HT1B, 5-HT1E, 5-HT1F, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT5A, and 5-HT7 receptors. Methylergometrine is an agonist of the serotonin 5-HT2B receptor
Methylergometrine
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Oxolinic_acid
Pharmaceutical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
DETQ
Pharmaceutical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
BP1.4979
Dopamine agonist medication
limbic areas. It is weakly active at the 5-HT2, and α2 receptors and is said to have virtually no affinity for the 5-HT1, GABA, mAChRs, α1-, and β-adrenoreceptors
Ropinirole
Chemical compound
and Therapeutics: 1039–1046. doi:10.1016/B978-1-4160-3291-5.50079-2. ISBN 978-1-4160-3291-5. Thiel, Verena; Brinkhoff, Thorsten; Dickschat, Jeroen S.;
Tropone
Chemical compound
(eds.). Gastroparesis. Elsevier. pp. 341–359. doi:10.1016/B978-0-12-818586-5.00025-9. ISBN 9780128185865. S2CID 225132800. Deudomperidone - AdisInsight
Deudomperidone
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Raclopride
Combination medication
March 2024. Retrieved 4 April 2024. "Details for: Vyalev". Health Canada. 5 February 2024. Retrieved 3 March 2024. "Notice: Multiple additions to the
Foscarbidopa/foslevodopa
Atypical antipsychotic medication
occupancy at 5-HT2A receptor are high at all doses (5 mg to 20 mg). It is reported that 5 mg dose of olanzapine produced a mean occupancy of 85% at 5 mg, 88%
Olanzapine
Dopamine agonist medication
antagonist, subtypes α2A and α2C. Lack of affinity to serotonin receptor 5-HT2B. "Active substance: piribedil" (PDF). List of nationally authorised medicinal
Piribedil
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Yangonin
Subfamily of dopamine receptors
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
D2-like_receptor
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
Α-Pyrrolidinopropiophenone
Atypical antipsychotic and antiemetic medication
oral tablets. In the United States, it is available in the form of a 5 mg/2 mL (2.5 mg/mL) solution for intravenous administration. Amisulpride's use is
Amisulpride
Typical antipsychotic drug of the thioxanthene class
patients treated with 5.7 ± 1.4 mg/day of flupentixol found 50-70% receptor occupancy for D2, 20 ± 5% for D1, and 20 ± 10% for 5-HT2A. Its antipsychotic
Flupentixol
Chemical compound
Fananserin Fenfluramine Iodobenzamide Isocorypalmine L-741,626 L-745,870 5-Hydroxyindoline Levofenfluramine LEK-8829 Metitepine (methiothepin) N-Methylspiperone
N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
Pharmaceutical compound
5-HT2A, 5-HT2C, and 5-HT2B receptors, an inverse agonist at the 5-HT7 receptor, a partial agonist at D2, D5, and 5-HT6 receptors, and an agonist at 5-HT1A
Nuciferine
Chemical compound in the ergot family of alkaloids
antimigraine drugs at 5‐HT receptors [...] TABLE 2 Summary of pEC50 values of cAMP (5‐HT1A/B/E/F and 5‐HT7), GTPγS (5‐HT1A/B/D/E/F), and IP (5‐HT2) assays of
Ergotamine
Antipsychotic medication
mostly affects the receptors of dopamine (D2), serotonin (5-HT2A, partially 5-HT1A, 5-HT2C, and 5-HT1D) and epinephrine/norepinephrine (α1) to a high degree
Ziprasidone
Serotonin dopamine partial agonist atypical antipsychotic
dopamine release that is triggered by 5-HT1A receptor agonism. It is also an antagonist of the serotonin 5-HT2A, 5-HT2B, and 5-HT7 receptors, which may contribute
Brexpiprazole
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
Female
Japanese
(1-æµ, 2-æ…¶, 3-æ¡‚, 4-敬, 5-å•“, 6-åœ, 7-景) Japanese name KEI means 1) "blessed, lucky," 2) "happy," 3) "katsura tree," 4) "respectful," 5) "spring," 6) "square jewel," or "sunny."Â
Surname or Lastname
South German (Düll)
South German (Düll) : nickname for a stubborn man.German (Düll) : variant of Dill 5.English : unexplained.
Male
Japanese
(1-æš, 2-悟, 3-è¡, 4-知, 5-覚, 6-è«, 7-了, 8-智) Japanese name SATORU means 1) "daybreak," 2) "enlightened," 3) "fast learner," 4) "knowledgeable," 5) "perceptive," 6) "persuasive," 7) "understanding," or 8) "wise."
Boy/Male
Muslim
One who prays 5 times and fasts, Forever, Immortal
Boy/Male
Hindu, Indian, Tamil
5 Head of Snake
Male
Japanese
(1-æ£, 2-é›…, 3-昌, 4-真, 5-政, 6-å°†) Unisex short form of Japanese names beginning with Masa-, MASA means 1) "correct, just," 2) "elegant, splendid" 3) "flourishing, prosperous" 4) "genuine, true," 5) "governing, political," 6) "military." Compare with another form of Masa.
Surname or Lastname
English
English : nickname from Middle English dull + -ard ‘dull or stupid person’. Compare Doll 5.Irish : either an importation to Ireland of the English name or, possibly, a reduced and altered form of de la Hyde (see Dollarhide).
Surname or Lastname
English
English : variant spelling of Peak.Irish : variant of Peak 2.North German : metonymic occupational name for a spearmaker, from Middle Low German pēk ‘pike’. Compare Pike 4.Dutch : variant of Peck 4 and 5.
Surname or Lastname
English
English : variant of Wall.Swedish : ornamental name composed of the elements wall, an old spelling of vall ‘grassy bank’ + man ‘man’.German (Wallmann) : variant of Wall 4 and 5.
Female
Japanese
(1-æ£, 2-é›…, 3-昌, 4-真, 5-政, 6-å°†) Unisex short form of Japanese names beginning with Masa-, MASA means 1) "correct, just," 2) "elegant," 3) "flourishing, prosperous" 4) "genuine, true," 5) "governing, political," 6) "military." Compare with strictly masculine Masa.
Surname or Lastname
English
English : occupational name for a maker or seller of hoods, from Middle English hodestre, a feminine form of Hodder.German (also Höster) : habitational name for someone from either of two places called Host (see Host 5).
Female
Japanese
(1-æµå, 2-æ…¶å, 3-æ¡‚å, 4-敬å, 5-å•“å, 6-åœå, 7-景å) Japanese name KEIKO means 1) "blessed, lucky child," 2) "happy child," 3) "katsura tree child," 4) "respectful child," 5) "spring child," 6) "square jewel child," or 7) "sunny child."
Girl/Female
Assamese, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
A Garland of 5 Types of Flowers
Surname or Lastname
German
German : diminutive of Summer 5.English (Bedfordshire) : unexplained.
Male
Japanese
(1-晋, 2-信, 3-紳, 4-心, 5-慎, 6-新, 7-進, 8-真) Japanese name SHIN means 1) "advancing," 2) "belief," 3) "gentleman," 4) "heart," 5) "humble," 6) "new," 7) "progressive," and 8) "true." Compare with another form of Shin.
Surname or Lastname
English (Yorkshire)
English (Yorkshire) : unexplained.French : from a diminutive of Bard 5.Hungarian (Bárdy) : habitational name for someone from a place called Bárd in Somogy county or in Máramaros, (now Maramures in Romania).
Surname or Lastname
English
English : patronymic from Kay 5.
Surname or Lastname
English
English : variant spelling of Kay 4 and 5.
Male
Japanese
(1-æµ, 2-ä½³, 3-敬, 4-åœ, 5-æ…§) Japanese name KEI means 1) "blessed, lucky," 2) "excellent," 3) "respect," 4) "square jewel," or 5) "wise."
Male
Japanese
(1-ç´€, 2-ä¿®, 3-ç†, 4-åŽ, 5-æ²», 6-çµ±) Japanese name OSAMU means 1) "chronicler," 2) "disciplined," 3) "logical," 4) "obtainer," 5) "to reign," 6) "ruler."
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
Boy/Male
Hindu, Indian, Marathi
The Sun; Light
Girl/Female
Muslim
One who travels
Girl/Female
Tamil
New
Boy/Male
Irish
Stranger.
Boy/Male
Muslim
8th Persian month
Boy/Male
English
Close to beech trees.
Boy/Male
Arabic, Kashmiri
Servant of the Giver
Girl/Female
British, English
Dear Beloved Friend
Boy/Male
Tamil
Palm tree
Boy/Male
Christian, Gujarati, Hindu, Indian, Malayalam, Tamil
God; God of Weather; Lord Shiva
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
5 HYDROXYINDOLINE
n.
See Tailing, n., 5.
a.
Affected with the vapors. See Vapor, n., 5.
n.
A morality play. See Morality, 5.
n.
See 4th Trap, 5.
n.
Same as Relief, n., 5.
v.
See Affected, 5.
n.
See Relief, n., 5.
n. & v.
See Prize, n., 5. Also Prize, v. t.
n.
See Tread, n., 5.
n.
Same as Reed, n., 5.
pref.
On; along; in traversing. Compare 5.
n.
Same as Placard, 4 & 5.
n.
An umbilicus. See Umbilicus, 5 (b).
n.
Same as Gudgeon, 5.
n.
See Camp, n., 5.
n.
See Romance, 5.
n.
A way for passage; a hall. See Passage, 5.
n.
See Flyer, n., 5.
n.
See Closure, 5.
n.
The thorax of an insect. See Trunk, n., 5.