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Chemical compound
4'-Hydroxyflavanone is a naturally occurring monohydroxybenzoic acid and a member of the 4'-hydroxyflavanones family. It is white to pale orange in color
4'-Hydroxyflavanone
Opioid receptor antagonist
2 hours, 44% at 4 hours, and 8% at 8 hours. A low dose (2 μg/kg) produced brain MOR blockade of 42% at 5 minutes, 36% at 2 hours, 33% at 4 hours, and 10%
Naloxone
Atypical opioid analgesic
found the binding affinity of 7-OH-MIT to be μ-opioid receptor (MOR) 37 (± 4) nM and δ-opioid receptor (DOR) 91 (± 8) nM and κ-opioid receptor (KOR) 132
7-Hydroxymitragynine
Species of plant
surfaces, and can grow to over 14–20 cm (5.5–7.9 in) long and 7–12 cm (2.8–4.7 in) wide. They have 12 to 17 pairs of veins. The spherical inflorescences
Mitragyna_speciosa
Cough suppressant and dissociative drug
Major Depressive Disorder". Clinical Psychopharmacology and Neuroscience. 21 (4): 609–616. doi:10.9758/cpn.23.1081. PMC 10591164. PMID 37859435. Kukanich
Dextromethorphan
Species of flowering plant in the poppy family
(L-DOPA), or it can be reduced to form 4-phenylhydroxyacetaldehyde (4-HPAA). Subsequently, L-DOPA reacts with 4-HPAA and, through a series of reactions
Papaver_somniferum
Opioid drug used in pain relief
minutes and lasts about 4–8 hours. The manufacturer's information says onset of action is about 10–30 minutes and duration is about 4–6 hours. Recommended
Hydrocodone
Opiate and prodrug of morphine used to treat pain
Panadeine, and the Tylenol-with-codeine series, including Tylenol 3 and 1, 2, and 4); with aspirin (as co-codaprin); or with ibuprofen (as Nurofen Plus). These
Codeine
Opioid medication used for pain relief
times as potent as morphine; although the conversion ratio may vary from 4–8 times, five times is in typical clinical usage. Patients with renal abnormalities
Hydromorphone
Species of plant
of kavain in blood specimens. The principal urinary metabolite, conjugated 4'-OH-kavain, is generally detectable for up to 48 hours. Kavalactones are quickly
Kava
Chemical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
MGM-15
Recreational drug beverage
Arthur, Texas, and member of the rap duo UGK, was found dead on December 4, 2007, at the Mondrian Hotel in West Hollywood, California. The Los Angeles
Lean_(drug)
Psychoactive component of cannabis
in a coffee shop". Journal of Analytical Toxicology. 34 (4): 196–203. doi:10.1093/jat/34.4.196. PMID 20465865. Baselt R (2011). Disposition of Toxic
Tetrahydrocannabinol
Psychoactive substance found in plants in the family Apocynaceae
3 hours and has a duration of 4 to 8 hours; the second phase is the evaluative or introspective phase, which starts after 4 to 8 hours and has a duration
Ibogaine
Chemical compound
nitazene analogs and their positional isomers". Drug Testing and Analysis. 15 (4): 449–457. doi:10.1002/dta.3415. PMID 36437623. S2CID 254042990. Papsun DM
Protonitazene
Tincture of opium
enema] every six to twelve hours"; (2) Tincture rhubarb, 1 ounce; Laudanum 4 drachms; "Dose: One teaspoonful every three hours." In a section entitled
Laudanum
Dissociative hallucinogenic drug, mostly used recreationally
treatment of phencyclidine psychosis". Journal of Clinical Pharmacology. 24 (4): 202–4. doi:10.1002/j.1552-4604.1984.tb01831.x. PMID 6725621. S2CID 42278510
Phencyclidine
Combination pain relief drug
of analgesia is about 20 to 30 minutes with a duration of 4 to 8 hours and t1/2 of 3 to 4 hours. Maximum serum levels are achieved at 1.3 hours. Metabolism/excretion:
Hydrocodone/paracetamol
Synthetic opioid analgesic
1007/s11419-017-0379-4. PMC 5754389. PMID 29367860. "Report on the risk assessment of methyl 1-(2-phenylethyl)-4-[phenyl(propanoyl) amino]piperidine-4-carboxylate
Carfentanil
Medication
hydrochloride tablet, extended release". DailyMed. 4 November 2021. Archived from the original on 4 June 2020. Retrieved 13 June 2022. "Vivitrol- naltrexone
Naltrexone
Medication used to treat ADHD
therapeutic effects of atomoxetine usually take 1 to 4 weeks to become apparent. A further 2 to 4 weeks may be required for the full therapeutic effects
Atomoxetine
Opioid medication
chronic pain syndromes. Oxycodone can be taken in an immediate-release form (4 times daily for example with the brand name Shortec) or twice daily with extended-release
Oxycodone
Semi-synthetic opioid, morphine analogue
original on 4 March 2016. Retrieved 4 May 2015. "DEA Diversion Control Division". Archived from the original on 2 March 2016. Retrieved 4 May 2015. Haskin
Desomorphine
Toxicity due to excessive consumption of opiates
Consult -- Online. Elsevier Health Sciences. p. PT4876. ISBN 978-1-4377-2129-4. Rosenblum A, Marsch LA, Joseph H, Portenoy RK (October 2008). "Opioids and
Opioid_overdose
Opioid analgesic of benzenoid class
Analgesia occurs within 32 minutes of oral administration, and lasts for 4–6 hours. Tapentadol is taken by mouth, and is available in immediate-release
Tapentadol
Chemical compound
4-Caffeoyl-1,5-quinide (4-caffeoylquinic-1,5-lactone or 4-CQL) is found in roasted coffee beans. It is formed by lactonization of 4-O-caffeoylquinic acid
4-Caffeoyl-1,5-quinide
Atypical opioid drug
piperidine 4-benzimidazolone derivative. It is structurally related to designer opioids such as brorphine. SR-17018 is highly lipophilic, with a log P of 4.75
SR-17018
Opioid analgesic and maintenance therapy
channel. Plasma concentrations of methadone in recovering addicts can reach 4 μM during therapy, so the actions of methadone at both the hERG potassium
Methadone
Type of α-amino acid
dihydroxyboryl derivative of phenylalanine, used in neutron capture therapy. 4-Azido-L-phenylalanine is a protein-incorporated unnatural amino acid used
Phenylalanine
Chemical compound
synthetic analogue of a fragment of adrenocorticotropic hormone (ACTH), ACTH (4-10), of the following amino acid sequence: Met-Glu-His-Phe-Pro-Gly-Pro (MEHFPGP
Semax
Atypical antidepressant
5 to 3 hours. The elimination half-life has been found to be increased to 4 to 9 hours in the elderly. Tianeptine is usually packaged as a sodium salt
Tianeptine
Off-label, experimental use of the drug
addiction treatment dosage. Most published research suggests a daily dosage of 4.5 mg, but this can vary by a few milligrams. LDN has been studied for the
Low-dose_naltrexone
Comparison of equivalent doses of pain medications
elimination half-lives of racemic tramadol and racemic M1 are 6.3 ± 1.4 and 7.4 ± 1.4 hours, respectively. The plasma elimination half-life of racemic tramadol
Equianalgesic
Impure form of heroin
severity of chronic venous disorders". Wound Repair and Regeneration. 17 (4): 485–491. doi:10.1111/j.1524-475X.2009.00513.x. ISSN 1067-1927. PMC 2748060
Black_tar_heroin
Substance derived from opium
and 20 million people used opioids recreationally, representing 0.3% to 0.4% of the global population between the ages of 15 and 65. According to the
Opiate
Opioid used to treat pain and opioid use disorder
ISBN 978-3-540-17471-4. Hutchinson MR, Zhang Y, Shridhar M, Evans JH, Buchanan MM, Zhao TX, et al. (January 2010). "Evidence that opioids may have toll-like receptor 4 and
Buprenorphine
Opioid analgesic
Parafluorofentanyl (4-fluorofentanyl, para-fluorofentanyl, pFF) is an opioid analgesic analogue of fentanyl developed by Janssen Pharmaceuticals in the
Parafluorofentanyl
Opioid medication
synthesis of N-phenethyl-4-piperidone (NPP). This intermediate is reductively aminated to 4-anilino-N-phenethylpiperidine (4-ANPP). Fentanyl is produced
Fentanyl
Opioid analgesic
4-Phenylfentanyl is an opioid analgesic that is a derivative of fentanyl. It was developed during the course of research that ultimately resulted in super-potent
4-Phenylfentanyl
Chemical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
7-Acetoxymitragynine
Dissociative anesthetic and anti-depressant
unusual clinical uses". British Journal of Anaesthesia. 77 (4): 441–4. doi:10.1093/bja/77.4.441. PMID 8942324. Orser BA, Pennefather PS, MacDonald JF (April
Ketamine
Chemical compound
opioids. Brorphine was originally reported to be highly biased, with an EC50 of 4.8nM for GTPγS binding and 182nM for β-arrestin recruitment, however a more
Brorphine
Medieval medical concoction
Ritva (Pesahim 45b), Rabbenu Manoah (Mishneh Torah, Hilchot Chametz u'Matzah 4:10), and Shulchan Aruch, Orah Haim 442 Di Gennaro Splendore, Barbara (2025)
Theriac
Traditional patent medicine
properties. According to Goodman and Gilman's 1965 edition, "Paregoric is a 4% opium tincture in which there is also benzoic acid, camphor, and anise oil
Paregoric
Chemical compound
pretreated with PCPA]". Eksperimental'naia i Klinicheskaia Farmakologiia. 72 (4): 6–8. PMID 19803361. Inozemtseva LS, Karpenko EA, Dolotov OV, Levitskaya
Selank
Protein-coding gene in the species Homo sapiens, named for ketazocine
the Terminals of the Neural Lobe". Endocrinology. 122 (4): 1321–1327. doi:10.1210/endo-122-4-1321. PMID 2894296. Zhao BG, Chapman C, Bicknell RJ (October
Κ-opioid_receptor
Compound medication
Behavioral Neurosciences. Vol. 34. pp. 59–75. doi:10.1007/7854_2015_422. hdl:1959.4/unsworks_62273. ISBN 978-3-319-60014-7. PMID 26768736. "Codeine Use While
Codeine/paracetamol
Dried latex of the opium poppy containing narcotic compounds
the original on July 6, 2022. Retrieved May 4, 2007. "The devil's doctor". April 18, 2006. Retrieved May 4, 2007. "PARACELSUS, Five Hundred Years: Three
Opium
Opioid analgesic compound
profiles of the µOR activated by diverse agonists". Nature Chemical Biology. 19 (4): 423–430. doi:10.1038/s41589-022-01208-y. PMC 11098091. PMID 36411392. S2CID 245021836
Mitragynine_pseudoindoxyl
Opioid analgesic
such as β-hydroxyfentanyl, ohmefentanyl, β-hydroxythiofentanyl and β-hydroxy-4-methylfentanyl. The development of such a wide structural family of novel
Α-Methylfentanyl
Opioid
rapidly with mean peak concentration at 1.7 hours. The mean half-life is 4 hours. The mean bioavailability of orally administered drug is 21%. Metabolite
Dihydrocodeine
Medical condition
risk of misuse and adverse effects. Long-term opioid use occurs in about 4% of people following their use for trauma or surgery-related pain. In the
Opioid_use_disorder
Portion of opium poppy
Sweden were found to have been lanced 2 – 5 times with a tool having 3 to 4 blades and the opium scraped off. The morphine content of these capsules was
Poppy_straw
Semi-synthetic opioid
etorphine. A 5–15 mg dose is enough to immobilise an African elephant and a 2–4 mg dose is enough to immobilise a black rhinoceros. Etorphine is a potent
Etorphine
Opiate alkaloid constituent of opium
Chemistry. pp. 46–54. doi:10.1002/14356007.a01_353.pub2. ISBN 978-3-527-30385-4. Vadhel, Agrataben; Bashir, Sabreen; Mir, Ashiq Hussain; Girdhar, Madhuri;
Thebaine
Chemical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Morphine_methylbromide
Synthetic opioid painkiller
[139943-10-5] (3). The Diels-Alder reaction with ethyl atropate [22286-82-4] (4) yields a mixture of isomers, of which only the (E)-(trans)-isomers are
Tilidine
Chemical substance with psychoactive properties
Pharmacology. XII. Classification of opioid receptors". Pharmacological Reviews. 48 (4): 567–92. PMID 8981566. Dickenson, A H (1991). "Mechanisms of the analgesic
Narcotic
Pharmaceutical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Deuterated_mitragynine
Octapeptide that mimics natural somatostatin pharmacologically
Endocrinology and Metabolism. 10 (1): 163–176. doi:10.1016/s0950-351x(96)80362-4. hdl:1765/60433. PMID 8734455. "Chiasma Announces FDA Approval of Mycapssa
Octreotide
Species of plant
(often also dentate) leaves, with a yellow undertone that reach 10 to 30 cm (4 to 12 in) long. The leaves have no hairs on either surface, and little or
Salvia_divinorum
Peptide hormone and neuropeptide
for oxytocin, as well as the preparation of analogues of the hormone (e.g. 4-deamido-oxytocin) was performed in the following decade by Iphigenia Photaki
Oxytocin
Organic compound used as flavouring and analgesic
Tissues of the Nose: Quantitative Studies". Archives of Otolaryngology. 38 (4): 309–317. doi:10.1001/archotol.1943.00670040323001. ISSN 0276-0673. Eccles
Menthol
Chemical compound
4-Fluoroisobutyrylfentanyl (also known as 4-FIBF and p-FIBF) is an opioid analgesic that is an analog of butyrfentanyl and structural isomer of 4-Fluorobutyrfentanyl
4-Fluoroisobutyrfentanyl
Chemical compound
Both active and inactive metabolites are excreted, mostly via the kidney (81.4%), and to a lesser extent via the feces (8%). In France, Portugal and Spain
Racecadotril
Chemical compound
4′,7-Dihydroxyflavone is a flavone. It is found in Medicago truncatula in relation with the root nodulation symbiont Sinorhizobium meliloti or in seeds
4',7-Dihydroxyflavone
Synthetic opioid analgesic
with remifentanil and its context-sensitive half-life remains at 4 minutes after a 4-hour infusion. Remifentanil is metabolized to a compound (remifentanil
Remifentanil
Chemical compound
oxime-substituted nitrosoalkene to generate the tetracyclic skeleton of conolidine in 4 steps. Takayama and colleagues (2016) synthesized conolidine and apparicine
Conolidine
Withdrawn opioid medication
propoxyphene induced shock". Journal of Toxicology. Clinical Toxicology. 23 (4–6): 353–6. doi:10.3109/15563658508990644. PMID 4057325. Holland DR, Steinberg
Dextropropoxyphene
Opioid analgesic drug
after oral administration it begins after about 30 minutes and lasts about 3–4 hours for immediate-release tablets and 12 hours for extended-release tablets
Oxymorphone
Opioid analgesic
in research. U-47700 is an agonist of the μ-opioid receptor (Ki 11.1 ± 0.4 nM) and possesses significantly lower affinity for the κ-opioid receptor (Ki
U-47700
Opioid analgesic and recreational drug
"Heroin-associated nephropathy". Expert Opinion on Drug Safety. 4 (1): 19–28. doi:10.1517/14740338.4.1.19. PMID 15709895. Offiah C, Hall E (February 2008). "Heroin-induced
Heroin
Opioid treatment
have the highest bioavailability. For example, a single dose of Bunavail 4.2 mg/0.7 mg achieves a Cmax around 3.41 ng/mL. Buprenorphine is metabolized
Buprenorphine/naloxone
Chemical compound
functional characterization of isotonitazene". Drug Testing and Analysis. 12 (4): 422–430. doi:10.1002/dta.2738. PMID 31743619. S2CID 208187034. Casy AF,
Isotonitazene
Chemical compound
shown that salvinorin A is a potent κ-opioid receptor (KOR) agonist (Ki = 2.4 nM, EC50 = 1.8 nM). It has a high affinity for the receptor, indicated by
Salvinorin_A
Pentapeptide
organization of the human preproenkephalin gene". Nature. 297 (5865): 431–4. Bibcode:1982Natur.297..431N. doi:10.1038/297431a0. PMID 6281660. S2CID 4371340
Enkephalin
Group of biological receptors
48 (4): 567–92. PMID 8981566. Janecka A, Fichna J, Janecki T (2004). "Opioid receptors and their ligands". Current Topics in Medicinal Chemistry. 4 (1):
Opioid_receptor
Class of opioid receptors found in humans
diverse actions of morphine". The Journal of Clinical Investigation. 127 (4): 1561–1573. doi:10.1172/JCI88760. PMC 5373896. PMID 28319053. Eisenberg RM
Mu-opioid_receptor
Classification of chemicals that directly modulate opioid neuropeptide systems
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Opioidergic
Chemical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Β-Neoendorphin
Opioid analgesic compound
The solubility of mitragynine in acidic water is higher (3.5 mg/ml at pH 4), however, this alkaloid can become unstable, so certain products, such as
Mitragynine
Herbal tea made out of poppy straw or poppy seeds
Home-Brewed Poppy Seed Tea by LC-MS/MS". Journal of Forensic Sciences. 63 (4): 1229–1235. doi:10.1111/1556-4029.13664. ISSN 0022-1198. PMID 28973785. S2CID 206919379
Poppy_tea
Pharmaceutical compound
4-Allyl-6-oxa-noribogainalog is a κ-opioid receptor (KOR) agonist of the oxa-ibogalog family related to oxa-noribogaine. It is a highly potent full agonist
4-Allyl-6-oxa-noribogainalog
Comprehensive list of compounds structurally related to fentanyl
reacting the ring structure as a base, 4-ANPP also called 4-anilino-N-phenethylpiperidine and despropionylfentanyl. 4-ANPP acts as a base because of its two
List_of_fentanyl_analogues
Metabolite of heroin
Neuro-Psychopharmacology & Biological Psychiatry. 8 (4–6): 747–50. doi:10.1016/0278-5846(84)90051-4. PMID 6543399. S2CID 23566872. Kapur BM, Aleksa K (December
6-Monoacetylmorphine
Medication
and Drug Administration (FDA) New Drug Application (NDA) for approval on 4 September 2018; the application was endorsed by an FDA advisory panel on 12
Esketamine
Synthetic Opioid pain medication
more of acute withdrawal symptoms can occur as opposed to typically 3 or 4 days for other codeine analogs. The clinical presentation in overdose cases
Tramadol
Chemical compound
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
IC-26
Medication for treatment of obesity
contains 8 mg naltrexone and 90 mg bupropion. Once full dosing is reached (after 4 weeks of administration), the total dosage of Contrave for treating overweight
Naltrexone/bupropion
Pain medication of the opiate family
pathway. Usually, the p38 within the dendritic cell expresses TLR 4 (toll-like receptor 4), which is activated through the ligand LPS (lipopolysaccharide)
Morphine
Receptor antagonist that acts on one or more of the opioid receptors
StatPearls Publishing, PMID 30725764, retrieved 2025-10-26 Fentanyl. Image 4 of 17. US DEA (Drug Enforcement Administration). See archive with caption:
Opioid_antagonist
Medication made from the peptide oxytocin
practice #4: avoid interventions unless they are medically necessary". The Journal of Perinatal Education. 23 (4): 198–206. doi:10.1891/1058-1243.23.4.198.
Oxytocin_(medication)
Synthetic opioid analgesic drug
Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 16 August
Sufentanil
Opioid antitussive and analgesic drug
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Nicodicodine
Synthetic opioid analgesic
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Alfentanil
Medicine used to reduce diarrhea
WF, et al. (July 1973). "Synthetic antidiarrheal agents. 2,2-Diphenyl-4-(4'-aryl-4'-hydroxypiperidino)butyramides". Journal of Medicinal Chemistry. 16 (7):
Loperamide
Semi-mythical remedy
(3S,4S)-Picenadol 2-(S)-N,N-(R)-Viminol 3CS-nalmefene 4-Caffeoyl-1,5-quinide 4′-Hydroxyflavanone 4',7-Dihydroxyflavone 6β-Naltrexol 6β-Naltrexol-d4 18-MC
Mithridate
Opioid analgesic
4-Fluorobutyrylfentanyl (also known as 4-FBF and p-FBF or para-fluorobutyrylfentanyl) is an opioid analgesic that is an analog of butyrfentanyl and has
4-Fluorobutyrfentanyl
Opioid analgesic
been reported in parrots and rabbits. Butorphanol when administered at 0.4 mg/kg given IV/IM does not provide sufficient post-operative analgesia for
Butorphanol
Chemical compound
(Nitazene Analog) Use: A Systematic Review". Therapeutic Drug Monitoring. 44 (4): 494–510. doi:10.1097/FTD.0000000000000970. PMID 35149665. S2CID 246776288
Etonitazepyne
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
Surname or Lastname
English
English : variant of Hearn 4.
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."
Boy/Male
Sikh
Who is always victorious, Winner from 4 directions, Perfectly victorious
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
Surname or Lastname
English
English : variant of Lyon 3.Irish : variant of Lyon 4.
Surname or Lastname
English
English : patronymic from Seal 4.
Surname or Lastname
English
English : variant of Hearn 4. This is predominantly a MD name.
Surname or Lastname
English and Welsh
English and Welsh : variant of Bach 3 and 4.
Surname or Lastname
English
English : variant of Hearn 2 and 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 spelling of Hearn 4.
Surname or Lastname
English
English : variant spelling of Rock.German (Röcke) : variant of Rock 4.
Surname or Lastname
English
English : variant spelling of Kay 4 and 5.
Surname or Lastname
English
English : variant of Cave 1 or 4.
Surname or Lastname
English
English : patronymic from Seal 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."
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.
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
Girl/Female
Indian
Nature; Behaviour
Boy/Male
Hindu
Uplifter of the poor
Boy/Male
Indian
Duality
Girl/Female
Australian, Danish, Dutch, German, Hebrew, Swedish
Life; Form of Eve
Boy/Male
Italian Spanish
A place name.
Girl/Female
Indian, Punjabi, Sikh
Beauty Queen; Daughter of God
Boy/Male
Hindu, Indian, Islamic
Fighter; Cute
Boy/Male
Latin French
White.
Boy/Male
Indian, Punjabi, Sikh
Loving Devotion to God
Boy/Male
Teutonic
Lord of the home.
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
4 HYDROXYFLAVANONE
n.
See Assessment, 4.
n.
Sympathy. See Sympathy, 4.
n.
See Rose, n., 4.
n.
Same as Indentation, 4.
n.
Same as Cribbing, 4.
n.
Same as Presbytery, 4.
n.
Offset, n., 4.
n.
See Tierce, 4.
n.
See 1st Hag, 4.
n.
See Flyer, n., 4.
n.
Same as Tailing, 4.
p. p. & a.
Same as Relative, 4.
n.
Same as Wale, n., 4.
n.
See Gad, n., 4.
n.
See Slime, 4.
n.
See Waft, n., 4.
n.
See Galley, n., 4.
n.
See Grit, n., 4.
n.
See Umber, 4.
n.
See Mule, 4.