Searches , social queries for 4 NEMD
Search references for 4 NEMD. Phrases containing 4 NEMD
See searches and references containing 4 NEMD!
Search references for 4 NEMD. Phrases containing 4 NEMD
See searches and references containing 4 NEMD!4 NEMD
Chemical compound
4-NEMD is a potent sedative drug which acts as a selective alpha-2 adrenergic receptor agonist. It is closely related to dexmedetomidine but is several
4-NEMD
Atypical antipsychotic medication
of insomnia of 0.05 (95% CITooltip confidence interval –1.21 to 1.11) at 4 weeks of treatment, with the certainty of evidence rated as very low. Doses
Quetiapine
Alpha-adrenergic agonist
of successful central nervous system drugs". NeuroRx. 2 (4): 541–553. doi:10.1602/neurorx.2.4.541. PMC 1201314. PMID 16489364. Skingle M, Hayes AG, Tyers
Clonidine
Medication used to treat anxiety disorders
contribute to its clinical efficacy. It has a delayed onset of action of 2–4 weeks. Buspirone also has weak antagonistic effects at dopamine D2, D3, and
Buspirone
Amino acid
L-Tyrosine or tyrosine (symbol Tyr or Y) or 4-hydroxyphenylalanine is one of the 20 standard amino acids that are used by cells to synthesize proteins
Tyrosine
Antidepressant medication
CYP1A2 inducer, increased trazodone peak levels by 1.4-fold, trazodone area-under-the-curve levels by 2.4-fold, and decreased trazodone clearance by 50%. This
Trazodone
Antihypertensive drug
(4–10% frequency) side effects of prazosin include dizziness, headache, drowsiness, fatigue, weakness, palpitations, and nausea. Less frequent (1–4%)
Prazosin
Chemical compound
the settlement of cyprid larvae of Balanus improvisus". Biofouling. 16 (2–4): 191–203. Bibcode:2000Biofo..16..191D. doi:10.1080/08927010009378444. S2CID 85603381
Medetomidine
Protein family
inhibition, where transmitters inhibit further release by homotropic effects. 4-NEMD 7-Me-marsanidine (also I1 agonist) Agmatine (also I agonist, NMDA, 5-HT3
Alpha-2_adrenergic_receptor
Chemical compound which aids breathing
Journal. Retrieved 4 April 2020. Assael S. "Dan Duchaine: a founding father of the steroid movement". espn.com. ESPN. Retrieved 4 April 2020. Pluim BM
Clenbuterol
Medication used for high blood pressure and ADHD
posttraumatic stress disorder". Croatian Medical Journal. 49 (4): 459–475. doi:10.3325/cmj.2008.4.459. PMC 2525822. PMID 18716993. Kaminer D, Seedat S, Stein
Guanfacine
Hormone and medication
responses to exercise". Journal of Applied Physiology. 51 (4): 788–793. doi:10.1152/jappl.1981.51.4.788. PMID 6795164. Richter EA, Galbo H, Christensen NJ
Adrenaline
Serotonin modulator antidepressant
other serotonin receptors. Whereas vortioxetine has IC50 or EC50 values of 5.4 nM for the SERT and 12 nM for the 5-HT3 receptor, its values are 120 to 450 nM
Vortioxetine
Beta blocker drug
unopposed α-stimulation with selective beta blockers has been reported to be 0.4%, whereas no cases of unopposed α-stimulation have been reported with dual
Propranolol
Muscle relaxant medication
patent. The 5-chloro-2,1,3-benzothiadiazol-4-amine intermediate was a known compound, produced in three steps from 4-chlorophenylenediamine as shown. Treatment
Tizanidine
Medication for overactive bladder
overactive bladder and urinary incontinence". Expert Opinion on Drug Discovery. 9 (4): 433–448. doi:10.1517/17460441.2014.892923. PMID 24559030. S2CID 26424400
Mirabegron
Muscle relaxant medication
fibromyalgia symptoms, with a reported number needed to treat of 4.8 (meaning that 1 person out of every 4.8 benefits from treatment) for pain reduction, but no
Cyclobenzaprine
Medication class with multiple uses
needed] Trials have shown beta blockers reduce the absolute risk of death by 4.5% over a 13-month period. In addition to reducing the risk of mortality,
Beta_blocker
Nasal decongestant
selectivity ratios in alpha 2 adrenergic receptors of 151 for a2A vs a2B, 4.5 a2A vs a2C, and 33.9 a2B vs a2C. Making it a highly selective a2A agonist
Xylometazoline
Medication
stones. Tamsulosin, however, appears to be effective for stones more than 4 mm and less than 10 mm only. Tamsulosin is also used as an add-on treatment
Tamsulosin
Beta blocker medication
β1-adrenergic receptors in heart muscle cells, thereby decreasing the slope of phase 4 in the nodal action potential (reducing Na+ uptake) and prolonging repolarization
Metoprolol
Atypical antipsychotic medication
ema.europa.eu. European Medicines Agency. 4 June 2004. Archived from the original on 15 April 2024. Retrieved 4 July 2024. "Abilify Tablets, Orodispersible
Aripiprazole
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Bromoacetylalprenololmenthane
Chemical compound
nightmares. The experimental log P of nebivolol is 4.18 and its predicted log P ranges from 2.44 to 4.21. It is a highly lipophilic beta blocker. The drug
Nebivolol
Chemical compound
two drops of 0.5 mg/mL of tetryzoline eye drops (0.025–0.05 mg) at 0 hrs, 4 hrs, 8 hrs, and 12 hrs. Within a 24-hour time window, since the last dose
Tetryzoline
Typical antipsychotic medication
Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 16 August
Chlorpromazine
Blood pressure medication
lipophilic compound with an experimental log P of 3.8 to 4.19 and a predicted log P of 3.05 to 4.2. It showed the third highest predicted lipophilicity
Carvedilol
Antihistamine drug
"Hydroxyzine". United States National Library of Medicine (NLM). Retrieved 4 March 2020. "Hydroxyzine". Go.drugbank.com. Retrieved 9 June 2026. "Hydroxyzine"
Hydroxyzine
Antidepressant medication
Organization project". Expert Review of Anticancer Therapy. 2 (4): 365–376. doi:10.1586/14737140.2.4.365. PMID 12647979. S2CID 72195061. Clark MS, Smith PO,
Mirtazapine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Amidephrine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Arbutamine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Dapiprazole
Veterinary anesthetic, sedative and analgesic
common with recommended withholding periods of 1–5 days for dairy cattle and 4–10 days for meat cattle. Cattle are more sensitive to xylazine than horses
Xylazine
Antihypertensive medication
Pharmacokinetics of Moxonidine". Journal of Cardiovascular Pharmacology. 20 (Suppl. 4): S37–S41. doi:10.1097/00005344-199220004-00008. "Physiotens Tablets (moxonidine)
Moxonidine
Chemical compound
more selective for β2 receptors. Since there is no hydroxy group on position 4 of the benzene ring, the molecule is less susceptible to metabolism by the
Terbutaline
Psychedelic drug
potent psychological effects. LSD taken orally has an onset of action of 0.4 to 1.0 hours and a duration of 7 to 12 hours. In recreational settings it
LSD
Sedative medication
S2CID 20447722. Liu T. "BindingDB BDBM50085683 (+)-4-((S)-alpha,2,3-trimethylbenzyl)imidazole::4-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole::CH
Dexmedetomidine
Atypical antipsychotic medication
analog as a potential atypical antipsychotic agent: 4-[4-(4-chlorophenyl)-1,4-diazepan-1-yl]-1-(4-fluorophenyl)butan-1-one". Bioorganic & Medicinal Chemistry
Olanzapine
Short-acting bronchodilator used for acute asthma
either filtered out by the kidneys directly or is first metabolised into the 4′-O-sulfate, which is excreted in the urine. Salbutamol is sold as a racemic
Salbutamol
Beta blocker medication
exercise-related tachycardia, are apparent within 1 hour and are maximal within 2 to 4 hours following a single oral dose. The general effects of atenolol, including
Atenolol
Typical antipsychotic medication
The IUPAC name of haloperidol decanoate is [4-(4-chlorophenyl)-1-[4-(4-fluorophenyl)-4-oxobutyl]piperidin-4-yl] decanoate. Topical formulations of haloperidol
Haloperidol
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Denopamine
Sympathomimetic agent
to 4% of an oral dose of phenylpropanolamine is metabolized. Metabolites include hippuric acid (via oxidative deamination of the side chain) and 4-hydroxynorephedrine
Phenylpropanolamine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Brimonidine
Stimulant designer drug
4-Methylethcathinone or 4-MEC is a chemical that bears a chemical resemblance to mephedrone. Due to its similarity to mephedrone, it is thought to be
4-Methylethcathinone
Medication used to treat high blood pressure
unopposed α-stimulation with selective beta blockers has been reported to be 0.4%, whereas no cases of unopposed α-stimulation have been reported with dual
Labetalol
Serotonin dopamine partial agonist atypical antipsychotic
equal to 5% vs. placebo) were: upper respiratory tract infection (6.9% vs. 4.8%), akathisia (6.6% vs. 3.2%), weight gain (6.3% vs. 0.8%), and nasopharyngitis
Brexpiprazole
Class of medications
and reward deficiency syndrome". Neuropsychiatric Disease and Treatment. 4 (5): 893–918. doi:10.2147/NDT.S2627. PMC 2626918. PMID 19183781. Biederman
Tricyclic_antidepressant
Chemical compound
4'-Methyl-α-pyrrolidinopropiophenone (4-MePPP, MPPP or MαPPP) is a stimulant drug and substituted cathinone. It is structurally very similar to α-PPP
4'-Methyl-α-pyrrolidinopropiophenone
4'-Methyl-α-pyrrolidinopropiophenone
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Trimazosin
Chemical compound
Pinner reaction with alcoholic hydrogen chloride leads to the iminoether, (4). Treatment with ethylenediamine [107-15-3] (5) gives the imidazoline ring
Idazoxan
Antihypotensive medication
System. Elsevier. pp. 413–415. doi:10.1016/b978-012589762-4/50113-4. ISBN 978-0-12-589762-4. Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical
Midodrine
Chemical compound
non-specific edema (2%). Arrhythmias were encountered in 4.8%, palpitations in 4.3%, and angina pectoris in 1.4%. In a combination study with 2,000 patients also
Cabergoline
Antipsychotic medication
or intramuscular). The injectable versions are long-acting and last for 2–4 weeks. Common side effects include weight gain, drowsiness, fatigue, insomnia
Risperidone
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Nipradilol
Hormone used as a medicine
and noradrenaline in sheep blood". Veterinary Research Communications. 30 (4). Springer Science and Business Media LLC: 423–32. doi:10.1007/s11259-006-3244-1
Epinephrine_(medication)
Veterinary medication
Kaivosaari S, Salonen JS, Taskinen J (March 2002). "N-Glucuronidation of some 4-arylalkyl-1H-imidazoles by rat, dog, and human liver microsomes". Drug Metabolism
Atipamezole
Topical decongestant
4636. DE 1117588, Fruhstorfer W, Müller-Calgan H, "2-(2,6-dimethyl-3-hydroxy-4-tert-butyl-benzyl)-2-imidazoline, and acid addition salts thereof, and process
Oxymetazoline
Chemical compound
main active metabolite, diacetolol, are reached after 4 hours. Acebutolol has a half-life of 3 to 4 hours, and diacetolol a half-life of 8 to 13 hours.
Acebutolol
Tricyclic antidepressant
an octanol-water partition coefficient (pH 7.4) of 3.0, while the log P of the free base was reported as 4.92. Solubility of the free base amitriptyline
Amitriptyline
Class of drugs
in mice: Mediated by α2-adrenergic receptors". Drug Development Research. 4 (6): 655–660. doi:10.1002/ddr.430040608. "Detomidine | α2-adrenergic Agonist
Alpha-adrenergic_agonist
Class of compounds
of benign prostatic hyperplasia". Canadian Urological Association Journal. 4 (5): 310–316. doi:10.5489/cuaj.10124. ISSN 1911-6470. PMC 2950766. PMID 20944799
Alpha-1_blocker
Chemical compound
are preferred. Tolazoline binds to the a2 adrenergic receptor at a ratio of 4:1, the lowest of all a2 adrenergic receptor antagonists. Tolazoline activates
Tolazoline
Tricyclic antidepressant
imipramine, amitriptyline, and dosulepin (dothiepin), with Ki values of 1.4 nM, 4.3 nM, and 8.3 nM, respectively. In addition, clomipramine has a terminal
Clomipramine
Atypical antipsychotic medication
conditions of high security". Advances in Psychiatric Treatment. 6 (4): 252–260. doi:10.1192/apt.6.4.252. ISSN 1355-5146. Silva E, Till A, Adshead G (July 2017)
Clozapine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Hexoprenaline
Antihypertensive drug
2. This, when heated in the presence of 2-chloro-6,7-dimethoxyquinazolin-4-amine (1) undergoes direct alkylation to terazosin (3). A 2022 study suggests
Terazosin
Drug that stimulates a response from the adrenergic receptors
methylphenidate, atomoxetine, cocaine, and some amphetamine based stimulants such as 4-hydroxyamphetamine. Ephedrine Pseudoephedrine Droxidopa or L-DOPS L-DOPA Adrenergic
Adrenergic_agonist
Medication used to treat high blood pressure
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Guanabenz
Group of stereoisomers
of hypertension". Expert Opinion on Pharmacotherapy. 9 (4): 625–633. doi:10.1517/14656566.9.4.625. PMID 18312163. S2CID 42056694. Chapman N, Chen CY,
Doxazosin
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Levobunolol
Stimulant recreational drug
4'-Methoxy-α-pyrrolidinopropiophenone (MOPPP) is a stimulant designer drug of the pyrrolidinophenone class. It has the potential to produce euphoria,[citation
4'-Methoxy-α-pyrrolidinopropiophenone
4'-Methoxy-α-pyrrolidinopropiophenone
Class of G protein-coupled receptors
vasoconstriction". Journal of Veterinary Pharmacology and Therapeutics. 20 (4): 308–17. doi:10.1046/j.1365-2885.1997.00078.x. PMID 9280371. Sagrada A, Fargeas
Adrenergic_receptor
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Acetergamine
Antiarrythmic medication
Quinidine also blocks certain voltage-gated potassium channels (e.g., Kv1.4, Kv4.2, hERG, among others), acts as an antimuscarinic and alpha-1 blocker
Quinidine
Antihistamine medication
BDBM50017721 1-Methyl-4-(5H-dibenzo(a,d)cycloheptenylidene)piperidine::1-methyl-4-(5-dibenzo(a,e)cycloheptatrienylidene)piperidine::4-(5-dibenzo(a
Cyproheptadine
Chemical compound
YC, Hsiao CH (June 2006). "Comparing efficacies of 0.5% apraclonidine with 4% cocaine in the diagnosis of horner syndrome in pediatric patients". Journal
Apraclonidine
Type of drug
beta-adrenoceptor-blocking drug. British journal of clinical pharmacology, 3(4 Suppl 3), 681–684. Golan, D. E.; Tashjian, A. H.; Armstrong, E. J. (2011)
Adrenergic_antagonist
Dopamine agonist medication
d2-dopamine agonist for the treatment of type 2 diabetes". Diabetes Care. 34 (4): 789–794. doi:10.2337/dc11-0064. PMC 3064029. PMID 21447659. "Bromocriptine"
Bromocriptine
Atypical antipsychotic medication
reduction was sixfold in a study. Lurasidone [(3aR,4S,7R,7aS)-2-{(1R,2R)-2-[4-(1,2-benzisothiazol-3-yl) piperazin-1-ylmethyl]-cyclohexylmethyl}-hexahydro-4
Lurasidone
Sedating antihistamine
primarily as a strong antagonist of the H1 receptor (antihistamine, Ki = 1.4 nM) and a moderate mACh receptor antagonist (anticholinergic), and also has
Promethazine
Chemical compound in the ergot family of alkaloids
Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 15 August
Ergotamine
Chemical compound
Form- 2'4'xylidine, 4-N-Methyl-formidoyl) amino-meta-toluix acid, 4-Formamido-meta-toluic acid, 4- Acetamido- meta-toluic acid and 4- Amino- meta- toluic
Amitraz
Antihypertensive medication
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Rilmenidine
Chemical compound
and catalyzed by prenyltransferase 4-dimethylallyltryptophan synthase (DMATS), to form 4-L-dimethylallyltryptophan (4-L-DMAT). The DMAPP is derived from
Ergine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Ronactolol
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Bitolterol
Long-acting bronchiodilator
short-acting β2 agonists such as salbutamol (albuterol), which are effective for 4 h to 6 h. Formoterol has a relatively rapid onset of action compared to other
Formoterol
Minor cannabinoid
A Systematic Review and Meta-Analysis". Inflammatory Bowel Diseases. 24 (4): 680–697. doi:10.1093/ibd/izy014. PMID 29562280. News N (31 July 2024). "Cannabigerol
Cannabigerol
Typical antipsychotic medication
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Levomepromazine
Atypical antipsychotic medication
death (12 confirmed and 4 suspected cases), suicide (7 cases), and neuroleptic malignant syndrome (4 cases). Of the 32 deaths, 59.4% were in patients over
Paliperidone_palmitate
Related to catecholamines (dopamine, adrenaline and noradrenaline)
Knowledge and understanding in the 1960s, now, and in the future". Brain and Neuroscience Advances. 3: 4–8. doi:10.1177/2398212818810682. PMC 7058270. v t e
Catecholaminergic
Antihypertensive medication
facilitates micturition. The bioavailability is 64%, and the plasma half-life is 4 to 6 hours. The maximum plasma concentration is reached after approximately
Alfuzosin
Medication used for opioid withdrawal
quantitative pharmacology". Pharmacological Reviews. 55 (4): 597–606. doi:10.1124/pr.55.4.4. PMID 14657418. S2CID 1729572. Gerra G, Zaimovic A, Giusti
Lofexidine
Chemical compound
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Carbuterol
Chemical used as a nasal decongestant
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Tramazoline
Chemical compound
"Brovana- arformoterol tartrate solution". DailyMed. 13 May 2021. Retrieved 4 March 2022. Loh CH, Donohue JF, Ohar JA (March 2015). "Review of drug safety
Arformoterol
Therapeutic use of norepinephrine
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
Norepinephrine_(medication)
Chemical compound
O-glucuronidation, O-methylation, N-demethylation, and sulfation. Only 3–4% of the apomorphine is excreted unchanged and into the urine. The half-life
Apomorphine
Drug
thioridazine) Urapidil WB-4101 Zolertine α2 Agonists (R)-3-Nitrobiphenyline 4-NEMD 6-FNE Amitraz Apraclonidine Brimonidine CHF-1024 Clonidine Corbadrine Deoxyepinephrine
(R)-3-Nitrobiphenyline
travel, tourism, insurance
4 NEMD
4 NEMD
Surname or Lastname
English
English : patronymic from Seal 4.
Surname or Lastname
English
English : patronymic from Seal 4.
Surname or Lastname
English and Welsh
English and Welsh : variant of Bach 3 and 4.
Female
Japanese
(1-鈴, 2-零, 3-麗, 4-霊) Japanese name REI means 1) "bell," 2) "nothing, zero" or 3) "lovely," 4) "spirit."
Surname or Lastname
English
English : variant of Hearn 4. This is predominantly a MD name.
Surname or Lastname
English
English : variant of Cave 1 or 4.
Surname or Lastname
English
English : variant spelling of Rock.German (Röcke) : variant of Rock 4.
Female
Japanese
(1-æ, 2- 京, 3- å”, 4- 郷) Japanese unisex name KYOU means 1) "apricot," 2) "capital," 3) "cooperation," or 4) "village."Â
Surname or Lastname
English
English : variant of Hearn 2 and 4.
Boy/Male
Sikh
Who is always victorious, Winner from 4 directions, Perfectly victorious
Surname or Lastname
English
English : variant spelling of Kay 4 and 5.
Female
Japanese
(1-æ, 2- 京, 3- å”, 4- 郷) Variant spelling of Japanese unisex Kyou, KYO means 1) "apricot," 2) "capital," 3) "cooperation," or 4) "village."Â
Boy/Male
Sikh
Who is always victorious, Winner from 4 directions, Perfectly victorious
Surname or Lastname
English (mainly Yorkshire)
English (mainly Yorkshire) : patronymic from Seller 1–4.
Female
Japanese
(1-儀, 2-典, 3-則, 4-法) Japanese unisex name NORI means 1) "ceremony, regalia," 2) "code, precedent," 3) "model, rule, standard," 4) "law, rule."
Surname or Lastname
English
English : variant of Hearn 4.
Surname or Lastname
English
English : variant of Lyon 3.Irish : variant of Lyon 4.
Female
Japanese
(1-亮, 2-é¼, 3-è«’, 4-涼) Japanese unisex name RYO means 1) "brightness," 2) "distant," 3) "reality," 4) "refreshing."
Surname or Lastname
English
English : variant spelling of Ray 1–4.
Surname or Lastname
English
English : variant spelling of Hearn 4.
4 NEMD
4 NEMD
4 NEMD
4 NEMD
4 NEMD
4 NEMD
4 NEMD
travel, tourism, insurance