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Antiviral drug
algae, appears to have entry inhibitor properties. DCM205, is a small molecule based on L-chicoric acid, an integrase inhibitor. DCM205 has been reported
Entry_inhibitor
Medication used to treat a viral infection
transcriptase inhibitor commonly used to suppress HIV-1 infection. Unlike DAAs that target viral proteins, host targeting antivirals (HTAs) inhibit host proteins
Antiviral_drug
analogue RTI 1991 (FDA) Docosanol Herpes Simplex Entry inhibitor 2000 (FDA) Dolutegravir HIV Integrase inhibitor Doravirine (Pifeltro) HIV Merck & Co NNRTI
List_of_antiviral_drugs
HIV entry inhibitor discovered in 1986
Peptide T is an HIV entry inhibitor discovered in 1986 by Candace Pert and Michael Ruff, a US neuroscientist and immunologist. Peptide T, and its modified
Peptide_T
Protein found in red algae
deposited in the PDB. It has been shown in vitro to be a highly potent HIV entry inhibitor. It is currently being investigated as a potential microbicide for
Griffithsin
Antiviral medication
MBarek M, Warlich M, Lohse AW, Pollok JM, et al. (May 2013). "The entry inhibitor Myrcludex-B efficiently blocks intrahepatic virus spreading in humanized
Bulevirtide
reverse-transcriptase inhibitors (NRTI) as a "backbone" along with one non-nucleoside reverse-transcriptase inhibitor (NNRTI), protease inhibitor (PI) or integrase
Management_of_HIV/AIDS
transcriptase inhibitor and an integrase inhibitor, and was further used in 2011 by a team of researchers combining an integrase inhibitor with a CCR5 entry inhibitor
Portmanteau_inhibitor
5 mg/kg doses. Leronlimab is a lab-made antibody that functions as an entry inhibitor. Leronlimab binds to the CCR5 receptor on the CD4 cells, and interferes
CCR5_receptor_antagonist
Antiretroviral medication used to treat HIV
immune system (immune reconstitution syndrome). Fostemsavir is an HIV entry inhibitor and a prodrug of temsavir (BMS-626529). Fostemsavir is a human immunodeficiency
Fostemsavir
Antiretroviral drug
in safety between the maraviroc and placebo groups. Maraviroc is an entry inhibitor. Specifically, maraviroc is a negative allosteric modulator of the
Maraviroc
Molecule that blocks enzyme activity
inhibition the substrate and inhibitor cannot bind to the enzyme at the same time. This usually results from the inhibitor having an affinity for the active
Enzyme_inhibitor
Immune system protein
phenotype. Discovery and development of CCR5 receptor antagonists Entry inhibitor HIV tropism Stephen Crohn HIV immunity GRCh38: Ensembl release 89:
CCR5
Third-generation topical retinoid
computational study claims that adapalene can be used as a potential entry inhibitor for Omicron variant of SARS-CoV-2. Anvisa (31 March 2023). "RDC Nº
Adapalene
Monoclonal antibody
binds CD4, the primary receptor for HIV, and inhibits HIV from entering cells. It is a post-attachment inhibitor, blocking HIV from binding to the CCR5 and
Ibalizumab
receptor binding protein, mediating entry into host cells. It is a key target for the design of entry inhibitors and vaccine immunogens. Garcia JE, Puentes
Hepatitis C virus envelope glycoprotein E2
Hepatitis_C_virus_envelope_glycoprotein_E2
antagonists HIV/AIDS research Reverse-transcriptase inhibitor Protease inhibitor Entry inhibitor Merson, M.D.; Michael, H. (2006), "HIV–AIDS Pandemic
Discovery and development of nucleoside and nucleotide reverse-transcriptase inhibitors
Discovery_and_development_of_nucleoside_and_nucleotide_reverse-transcriptase_inhibitors
Viruses portal Discovery and development of CCR5 receptor antagonists Entry inhibitor HIV tropism Timothy Ray Brown Stephen Crohn Scutti, Susan (20 November
Innate_resistance_to_HIV
Monoclonal antibody
(N=62, p=.005). PRO 140 is a lab-made antibody that functions as an entry inhibitor. PRO 140 binds to the CCR5 receptor on the CD4 cells, and interferes
Leronlimab
Pharmaceutical compound
infection. This drug is a synthesized variant of a highly specific natural entry inhibitor designated as VIRIP (virus-inhibitory peptide). The design of VIR-576
VIR-576
History of molecular discovery
inhibitor Entry inhibitor Discovery and development of non-nucleoside reverse transcriptase inhibitors Discovery and development of NS5A inhibitors Cuccioloni
Discovery and development of HIV-protease inhibitors
Discovery_and_development_of_HIV-protease_inhibitors
Class of HIV/AIDS drugs
HIV-1 capsid protein, and the most promising peptide inhibitor was the capsid assembly inhibitor (CAI) peptide. CAI prevented the formation of mature
HIV_capsid_inhibition
Antiretroviral drug used to treat HIV
Enfuvirtide (INN), sold under the brand name Fuzeon, is an HIV fusion inhibitor, the first of a class of antiretroviral drugs used in combination therapy
Enfuvirtide
American biotechnology company
antiviral activity and resistance of a novel small molecule HIV-1 entry inhibitor". Bioorganic & Medicinal Chemistry. 23 (24): 7618–7628. doi:10.1016/j
CPC_Scientific
Chemical compound
Aplaviroc (INN, codenamed AK602 and GSK-873140) is a CCR5 entry inhibitor that belongs to a class of 2,5-diketopiperazines developed for the treatment
Aplaviroc
Type of drug
Endocannabinoid reuptake inhibitor TRPC6 activators (wide-spectrum reuptake inhibitors) – hyperforin, adhyperforin Choline reuptake inhibitor – hemicholinium-3
Reuptake_inhibitor
body. Another discovery made using HTS is Maraviroc. It is an HIV entry inhibitor, and slows the process and prevents HIV from being able to enter human
High_throughput_biology
Antiretroviral medication
(HAART). Ritonavir is a protease inhibitor, though it now mainly serves to boost the potency of other protease inhibitors. It may also be used in combination
Ritonavir
Virus mutation
resistance mutations can effect the efficacy of these treatments as well. Entry inhibitors block the ability of HIV to enter its target cells. HIV must bind to
Resistance mutation (virology)
Resistance_mutation_(virology)
Chemical compound
[citation needed] Cenicriviroc is an inhibitor of CCR2 and CCR5 receptors, allowing it to function as an entry inhibitor which prevents the virus from entering
Cenicriviroc
Chemical compound
Vicriviroc, previously named SCH 417690 and SCH-D, is a pyrimidine CCR5 entry inhibitor of HIV-1. It was developed by the pharmaceutical company Schering-Plough
Vicriviroc
American biologist (1944–2001)
Don C. (September 2000). "The structure of an HIV-1 specific cell entry inhibitor in complex with the HIV-1 gp41 trimeric core". Bioorganic & Medicinal
Don_Craig_Wiley
Class of drugs to lower cholesterol
dihydroxybergamottin) inhibit the cytochrome P450 enzyme CYP3A4, which is involved in the metabolism of most statins (however, it is a major inhibitor of only lovastatin
Statin
American geneticist
based association analysis. This discovery has led to several HIV entry inhibitor developments that have been approved by FDA as also stimulated the
Stephen_J._O'Brien
Antiretroviral medication
reverse-transcriptase inhibitor and an antiretroviral from another group, such as a protease inhibitor, non-nucleoside reverse-transcriptase inhibitor, or integrase
Zidovudine
Protein
has been shown to interact with USP14. CXCR4 antagonist HIV tropism Entry inhibitor Discovery and development of CCR5 receptor antagonists GRCh38: Ensembl
CXCR4
Enzyme
inhibitors are chelating agents. The inhibitor binds to the zinc at the active center of the enzyme, thereby blocking its activity. Other inhibitor mechanisms
Metalloprotease_inhibitor
American pharmacologist (born 1981)
mechanisms other than reverse transcriptase inhibition such as the HIV entry inhibitor maraviroc; she found that genetic variants of CYP3A genes could impact
Namandjé_Bumpus
Superfamily of proteins with similar structures and diverse functions
methionine in alpha1-antitrypsin as an inhibitor of tissue elastase and on arginine in antithrombin as an inhibitor of thrombin. The critical role of the
Serpin
HIV-infected individual who does not progress to immune deficiency
mechanism led to the development of a class of HIV medicines, the entry inhibitors. The presence of this mutation, however, is not a unifying theme among
Long-term_nonprogressor
Nuclear protein
be true) where Wee1 is a dosage-dependent inhibitor of Cdc2, whose activity is required for a cell's entry into M phase. As a result of these discoveries
Wee1
drug Reverse-transcriptase inhibitor Protease inhibitor Entry inhibitor Discovery and development of HIV-protease inhibitors Discovery and development
Discovery and development of non-nucleoside reverse-transcriptase inhibitors
Discovery_and_development_of_non-nucleoside_reverse-transcriptase_inhibitors
Glycoprotein exposed on the surface of the HIV virus
secretion in neuronal cells. HIV envelope gene HIV entry to the cell gp41 CD4 CCR5 Entry inhibitor Structure and genome of HIV Sodroski, Joseph; Patarca
Envelope_glycoprotein_GP120
Protein
Zappe H, Snell ME, Bossard MJ (2008). "PEGylation of cyanovirin-N, an entry inhibitor of HIV". Adv. Drug Deliv. Rev. 60 (1): 79–87. doi:10.1016/j.addr.2007
Cyanovirin-N
Invention of new medications based on knowledge of a biological target
COX-2 inhibitor NSAIDs Enfuvirtide, a peptide HIV entry inhibitor Nonbenzodiazepines like zolpidem and zopiclone Raltegravir, an HIV integrase inhibitor SSRIs
Drug_design
Enzyme that metabolizes substances by oxidation
clearance. a Moderate inhibitor causes at least a 2-fold increase in the plasma AUC values, or 50–80% decrease in clearance. a Weak inhibitor causes at least
CYP3A4
Pharmaceutical company
Pharmaceuticals]) Protease inhibitors: fosamprenavir (brand names Lexiva and Telzir) nelfinavir (brand name Viracept) Entry inhibitors: maraviroc (brand names
ViiV_Healthcare
American chemist and structural biologist
Zhao and B. Wu (2013) Structure of the CCR5 chemokine receptor-HIV entry inhibitor maraviroc complex Science 341: 1387-90 H. Wu, C. Wang, K. J. Gregory
Raymond_C._Stevens
Cell cycle regulator
Early Mitotic Inhibitor 1 (EMI1) is an important cell cycle regulator which ensures timely mitotic entry by primarily inhibiting Anaphase-Promoting Complex/Cyclosome
Early_Mitotic_Inhibitor_1
Pentacyclic chemical compound in plant leaves and fruit
2013). "Development of oleanane-type triterpenes as a new class of HCV entry inhibitors". Journal of Medicinal Chemistry. 56 (11): 4300–4319. doi:10.1021/jm301910a
Oleanolic_acid
Class of enzymes
Medroxyprogesterone acetate and medrogestone are weak inhibitors of 3β-HSD which may substantially inhibit it at high dosages.[citation needed] Human steroidogenesis
3β-Hydroxysteroid dehydrogenase
3β-Hydroxysteroid_dehydrogenase
2007). "The novel fold of scytovirin reveals a new twist for antiviral entry inhibitors". Journal of Molecular Biology. 369 (2): 451–61. doi:10.1016/j.jmb
Scytovirin
Pharmaceutical drug class
selective as a Bcr-Abl inhibitor and these changes resulted in the discovery of nilotinib. Nilotinib is a selective Bcr-Abl kinase inhibitor. Nilotinib is 10-30
Bcr-Abl tyrosine-kinase inhibitor
Bcr-Abl_tyrosine-kinase_inhibitor
Protein structural motif
An inhibitor cystine knot (also known as ICK or Knottin) is a protein structural motif containing three disulfide bridges. Knottins are one of three folds
Inhibitor_cystine_knot
Subunit of the envelope protein complex of retroviruses
36-residue alpha-peptide fusion inhibitor drug that binds to the pre-hairpin structure and prevents membrane fusion and HIV-1 entry to the cell. The vulnerability
Gp41
Canadian academic, doctor
women's control. He conducted placebo-controlled trials of an HIV entry inhibitor that was formulated as vaginal gel. After studying the experiment results
Michel_Alary
Infection specificity of pathogens
phagocytosis, and nonspecific inhibitors. An anatomical barrier is any physical or chemical barrier that helps prevent entry of microorganisms into body
Host_tropism
Drugs that inhibit β-Lactamase enzymes
A β-Lactamase inhibitor is a chemical compound that prevents bacterial degradation of β-lactam (beta-lactam) antibiotics. Beta-lactamases are a family
Β-Lactamase_inhibitor
Inhibitors of translation
A protein synthesis inhibitor is a compound that stops or slows the growth or proliferation of cells by disrupting the processes that lead directly to
Protein_synthesis_inhibitor
Sic1, a protein, is a stoichiometric inhibitor of Cdk1-Clb (B-type cyclins) complexes in the budding yeast Saccharomyces cerevisiae. Because B-type cyclin-Cdk1
Sic1
Protein-coding gene in the species Homo sapiens
T, et al. (October 2013). "Human MX2 is an interferon-induced post-entry inhibitor of HIV-1 infection". Nature. 502 (7472): 559–62. Bibcode:2013Natur
MX2
American biomedical researcher (born 1937)
to a class of drugs used to treat HIV, the chemokine antagonists or entry inhibitors, and helped (conceptually) in the advances that led to the discovery
Robert_Gallo
Immature soybean pod used as a specialty food
Beta-amylase Lipoxygenase Cysteine proteases Trypsin inhibitors Kunitz inhibitor Bowman-Birk inhibitor Other Soy lecithin (mix of Phospholipids) Lunasin
Edamame
Serine protease inhibitor
some viral infections, as well as inhibiting fibrosis in liver or kidney disease or pancreatitis. It is an inhibitor of the enzyme transmembrane protease
Camostat
Protein family
In molecular biology, ecotin is a protease inhibitor which belongs to MEROPS inhibitor family I11, clan IN. Ecotins are dimeric periplasmic proteins from
Ecotin
Science that studies the disease called herpes
Suzuki H (August 2011). "Effect of ASP2151, a herpesvirus helicase-primase inhibitor, in a guinea pig model of genital herpes". Molecules. 16 (9): 7210–23
Herpes_simplex_research
Class of enzymes
rather a mechanism of action class with diverse chemistries. The ALS inhibitor family includes sulfonylureas (SUs), imidazolinones, triazolopyrimidines
Acetolactate_synthase
Mammalian protein found in Homo sapiens
include non-covalent inhibitor complexes and covalent adducts. The slime mold Dictyostelium discoideum produces a semispecific FAAH inhibitor. By controlling
Fatty-acid_amide_hydrolase_1
Protein-coding gene in the species Homo sapiens
considered to be the predominant elastase inhibitor in secretions, while α1-antitrypsin is the predominant elastase inhibitor in tissues. Several diseases, including
SLPI
Medical treatment for newborns
and Gunn started by looking unsuccessfully at flunarizine, a calcium entry inhibitor. Edwards picked on nitric oxide synthase inhibition which was also
Hypothermia therapy for neonatal encephalopathy
Hypothermia_therapy_for_neonatal_encephalopathy
Earliest stage of infection in the viral life cycle
Viral entry is the earliest stage of infection in the viral life cycle, as the virus comes into contact with the host cell and introduces viral material
Viral_entry
Chemical compound
bunyavirus, flavivirus and filovirus families. It acts as an inhibitor which blocks viral entry into host cells. In animal tests FGI-106 shows both prophylactic
FGI-106
Protein-coding gene in the species Homo sapiens
secretory trypsin inhibitor (PSTI) also known as serine protease inhibitor Kazal-type 1 (SPINK1) or tumor-associated trypsin inhibitor (TATI) is a protein
SPINK1
Group of cells allowing a pathogen to infect nearby endothelium
Zhou, Yanchen; Simmons, Graham (October 2012). "Development of novel entry inhibitors targeting emerging viruses". Expert Review of Anti-infective Therapy
Endothelial_cell_tropism
Small molecules that inhibit the Hedgehog signaling pathway
sonidegib, both inhibitors of Smoothened (SMO), which are being used for the treatment of basal cell carcinoma. Arsenic trioxide, an inhibitor of GLI transcription
Hedgehog_pathway_inhibitor
German-Swiss biochemist and protein engineer
S. (2022). "Designed Ankyrin Repeat Proteins: A New Class of Viral Entry Inhibitors". Viruses. 14 (10): 2242. Hanes, J.; Plückthun, A. (1997). "In vitro
Andreas_Plückthun
DK, Lin L, Jenwitheesuk E, Samudrala R, Isern S, Michael SF. Viral entry inhibitors block dengue antibody-dependent enhancement in vitro. Antiviral Research
Ram_Samudrala
Drugs used in cancer treatment
PMID 8137252. "Tezacitabine monohydrate". Ribonucleotide reductase inhibitor entry in the public domain NCI Dictionary of Cancer Terms This article incorporates
Ribonucleotide reductase inhibitor
Ribonucleotide_reductase_inhibitor
Chemical compound
juice (which is a CYP3A4 inhibitor) increases the drug's maximum concentration by around 50%. Cilostazol is a selective inhibitor of phosphodiesterase type
Cilostazol
Chemical compound
Huang W, Wang Y (August 2022). "Screening and identification of HTNVpv entry inhibitors with high-throughput pseudovirus-based chemiluminescence". Virologica
Cepharanthine
Class of enzymes
children 12–18 were still covered under the EUA. The 3C-like protease inhibitor ensitrelvir received authorization to treat COVID-19 in Japan in 2022
3C-like_protease
Antiviral drug
an antiviral drug which is the first drug developed that acts by inhibiting viral entry into cells via macropinocytosis. While it is only in early developmental
Virapinib
Chemical compound
(loxistatin, E-64d, EST) is a drug which acts as a cysteine protease inhibitor and has anticoagulant effects. It is a synthetic analogue of E-64, a natural
Aloxistatin
Protein-coding gene in the species Homo sapiens
X-linked inhibitor of apoptosis protein (XIAP), also known as inhibitor of apoptosis protein 3 (IAP3) and baculoviral IAP repeat-containing protein 4 (BIRC4)
XIAP
Administration (United States) functional antibody – fungus – fusin – fusion inhibitor – fusion mechanism – fusion peptide GAG – gamma globulin – gamma interferon
Index of HIV/AIDS-related articles
Index_of_HIV/AIDS-related_articles
Regular measurement of the viral load of HIV-positive people
transcriptase inhibitors (NNRTIs) Nucleoside reverse transcriptase inhibitors (NRTIs) protease inhibitors (PIs) entry inhibitors Fusion inhibitors Integrase
Viral_load_monitoring_for_HIV
Set of three serine threonine-specific protein kinases
phase-2 trials AKT inhibitor AZD5363 well tolerated, yielded partial response in patients with advanced solid tumors "PARP/AKT Inhibitor Combination Active
Protein_kinase_B
Active region of an enzyme
site and an enzyme inhibitor. If the enzyme found in bacteria is significantly different from the human enzyme then an inhibitor can be designed against
Active_site
Chemical compound
isolated from actinomycetes and used in biochemical research as a protease inhibitor of trypsin and papain. It was discovered in 1972 and was the first natural
Antipain
Chemical compound
Apilimod (STA-5326) is a drug that was initially identified as an inhibitor of production of the interleukins IL-12 and IL-23, and developed for the oral
Apilimod
for HIV treatment relies on the genetic makeup of the individual. Entry inhibitors bind to the CCR5 protein to block HIV from binding to the CD4 cell
HIV_disease_progression_rates
Soy-based food used as a protein source
Beta-amylase Lipoxygenase Cysteine proteases Trypsin inhibitors Kunitz inhibitor Bowman-Birk inhibitor Other Soy lecithin (mix of Phospholipids) Lunasin
Tofu
Class of medications used to alleviate anxiety
of less sedating and withdrawal effects. The first monoamine oxidase inhibitor (MAOI), iproniazid, was discovered accidentally when developing the new
Anxiolytic
Mammalian protein found in humans
hypoglycemia, and recurrent infections. Cholesterol side-chain cleavage enzyme inhibitors include aminoglutethimide, ketoconazole, and mitotane, among others. Cholesterol
Cholesterol side-chain cleavage enzyme
Cholesterol_side-chain_cleavage_enzyme
Japanese food made from fermented soybeans
Beta-amylase Lipoxygenase Cysteine proteases Trypsin inhibitors Kunitz inhibitor Bowman-Birk inhibitor Other Soy lecithin (mix of Phospholipids) Lunasin
Nattō
Chemical compound
(2006). "Rapid Microwave-Assisted Syntheses of Derivatives of HIV-1 Entry Inhibitors". Synthesis. 2006 (5): 807–812. doi:10.1055/s-2006-926339. L. Tilley;
4-Amino-2,2,6,6-tetramethylpiperidine
4-Amino-2,2,6,6-tetramethylpiperidine
Species of virus affecting humans and animals
to inhibit Ebola virus infection by preventing viral envelope glycoprotein (GP) from binding to NPC1. Hence, NPC1 was shown to be critical to entry of
Zaire_ebolavirus
Commemorative coins of the Eurozone
million coins 3 January 2018 Description: The design symbolises Slovakia's entry into the European Union and the euro area by showing a stylised portal arching
2_euro_commemorative_coins
ACE angiotensin-converting enzyme ACEI angiotensin-converting enzyme inhibitor ACh acetylcholine AChE acetylcholine esterase ACL anterior cruciate ligament
List of medical abbreviations: A
List_of_medical_abbreviations:_A
Exopeptidase enzyme that acts on angiotensin I and II
them. Even low mACE2 levels can allow entry if TMPRSS2 is present. Rodent studies have shown that ACE inhibitors and angiotensin II receptor blockers (ARBs)
Angiotensin-converting enzyme 2
Angiotensin-converting_enzyme_2
ENTRY INHIBITOR
ENTRY INHIBITOR
Boy/Male
Hindu, Indian
An Entry Point into a Dispute
Girl/Female
Biblical
An entry or vestibule.
Surname or Lastname
English
English : habitational name from places in Lincolnshire and Nottinghamshire called Winthorpe. The former is named with the Old English personal name or byname Wine, meaning ‘friend’, + Old Norse þorp ‘settlement’. In the latter the first element is a contracted form of the Old English personal name Wigmund, composed of the elements wÄ«g ‘war’ + mund ‘protection’, or the Old Norse equivalent, VÃgmundr.John Winthrop (1588–1649) was the first governor of the Massachusetts Bay Colony. He kept a detailed journal, an invaluable source for historians. He was born into a family of Suffolk, England, gentry whose fortunes were founded by his grandfather Adam Winthrop (d. 1562) of Lavenham. In 1544 the latter acquired a 500-acre estate that had been part of the monastery of Bury St. Edmunds. John Winthrop emigrated from Groton, Suffolk, England, to Salem, MA, in 1630 because of Charles I’s anti-Puritan policies. By the time of his death he had had four wives and 16 children, the most notable of whom was his son John (1606–76), a scientist and governor of CT. His descendants were prominent in politics and science, including John Winthrop (1714–79), an astronomer, and Robert Winthrop (1809–94), a senator and speaker of the House of Representatives.
Biblical
an entry or vestibule
Surname or Lastname
English
English : unexplained.possibly an Americanized spelling of Italian Ventre, a short form of a compound name formed with ventre ‘belly’, ‘stomach’, such as Bonventre.
Surname or Lastname
English
English : variant spelling of Gent (see Gentry).
Girl/Female
Hindu, Indian
Entry
Surname or Lastname
English
English : habitational name from Raleigh in Devon, recorded in Domesday Book as Radeleia, from Old English rēad ‘red’ + lēah ‘wood’, ‘clearing’.The English explorer Sir Walter Raleigh (1554–1618) was born in Hayes Barton, Devon, into a family of Devon gentry. He was related to most of the West Country’s important families, including that of Sir Francis Drake. His half-brother was the explorer Sir Humphrey Gilbert. In 1578 Raleigh was granted a patent to explore and colonize “unknown lands†in America.
Surname or Lastname
English
English : nickname, sometimes perhaps ironic, from Middle English, Old French genterie ‘nobility of birth or character’. Compare Gentle.
Boy/Male
Arabic, Biblical
Helper; Entry-way
Biblical
helper; entry-way
Boy/Male
American, Australian, British, English, French, German, Latin
Sentry; Keeper of Grain; Surname
Boy/Male
Hindu, Indian, Tamil
Entry; Good in Look
Surname or Lastname
English
English : status name from Middle English squyer ‘esquire’, ‘a man belonging to the feudal rank immediately below that of knight’ (from Old French esquier ‘shield bearer’). At first it denoted a young man of good birth attendant on a knight, or by extension any attendant or servant, but by the 14th century the meaning had been generalized, and referred to social status rather than age. By the 17th century, the term denoted any member of the landed gentry, but this is unlikely to have influenced the development of the surname.
ENTRY INHIBITOR
ENTRY INHIBITOR
Girl/Female
Hindu, Indian, Marathi, Sanskrit
Young Woman; Maid
Girl/Female
Latin
Daughter of Halmus.
Boy/Male
Tamil
Rangaprasath | ரஂகபà¯à®°à®¸à®¾à®¤
Give the varam
Girl/Female
Muslim
Pure
Male
Serbian
Pet form of Serbian Vilim, VILKO means "will-helmet."
Boy/Male
Native American
Black kettle.
Boy/Male
Tamil
Satyavrath | ஸதà¯à®¯à®µà¯à®°à®¤
One who has taken vow of truth
Boy/Male
Arabic, Hindu, Indian, Marathi
King of the World; Moonlight
Girl/Female
Hindu, Indian, Traditional
Immortality
Boy/Male
Assamese, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Mythological, Telugu
Son of Dronacharya; Fiery; Tempered
ENTRY INHIBITOR
ENTRY INHIBITOR
ENTRY INHIBITOR
ENTRY INHIBITOR
ENTRY INHIBITOR
n.
The act of entering or passing into or upon; entrance; ingress; hence, beginnings or first attempts; as, the entry of a person into a house or city; the entry of a river into the sea; the entry of air into the blood; an entry upon an undertaking.
n.
That by which entrance is made; a passage leading into a house or other building, or to a room; a vestibule; an adit, as of a mine.
n.
See Sentry.
n.
The act in addition to breaking essential to constitute the offense or burglary.
n.
The actual taking possession of lands or tenements, by entering or setting foot on them.
n.
An erroneous entry or charge, as of an account.
pl.
of Sentry
n.
A putting upon record in proper form and order.
n.
Guard; watch, as by a sentinel.
n.
A second or new entry; as, a reentry into public life.
a.
Permissible; done lawfully; as, entry congeable.
n.
The entry of such adjournment and the grounds thereof on the record.
n.
A soldier placed on guard; a sentinel.
n.
The exhibition or depositing of a ship's papers at the customhouse, to procure license to land goods; or the giving an account of a ship's cargo to the officer of the customs, and obtaining his permission to land the goods. See Enter, v. t., 8, and Entrance, n., 5.
a.
People of education and good breeding; in England, in a restricted sense, those between the nobility and the yeomanry.
n.
The act of making or entering a record; a setting down in writing the particulars, as of a transaction; as, an entry of a sale; also, that which is entered; an item.
n.
A sentry.
n.
An additional or subsequent entry.
a.
Courtesy; civility; complaisance.
pl.
of Entry