List of benzodiazepines

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Template:Short description Template:Benzos The tables below contain a sample list of benzodiazepines and benzodiazepine analogs that are commonly prescribed, with their basic pharmacological characteristics, such as half-life and equivalent doses to other benzodiazepines, also listed, along with their trade names and primary uses. The elimination half-life is how long it takes for half of the drug to be eliminated by the body. "Time to peak" refers to when maximum levels of the drug in the blood occur after a given dose. Benzodiazepines generally share the same pharmacological properties, such as anxiolytic, sedative, hypnotic, skeletal muscle relaxant, amnesic, and anticonvulsant effects. Variation in potency of certain effects may exist amongst individual benzodiazepines. Some benzodiazepines produce active metabolites. Active metabolites are produced when a person's body metabolizes the drug into compounds that share a similar pharmacological profile to the parent compound and thus are relevant when calculating how long the pharmacological effects of a drug will last. Long-acting benzodiazepines with long-acting active metabolites, such as diazepam and chlordiazepoxide, are often prescribed for benzodiazepine or alcohol withdrawal as well as for anxiety if constant dose levels are required throughout the day. Shorter-acting benzodiazepines are often preferred for insomnia due to their lesser hangover effect.[1][2][3][4][5]

It is fairly important to note that elimination half-life of diazepam and chlordiazepoxide, as well as other long half-life benzodiazepines, is twice as long in the elderly compared to younger individuals. Due to increased sensitivity and potentially dangerous adverse events among elderly patients, it is recommended to avoid prescribing them as specified by the 2015 American Geriatrics Society Beers Criteria.[6] Individuals with an impaired liver also metabolize benzodiazepines more slowly. Thus, the approximate equivalent of doses below may need to be adjusted accordingly in individuals on short acting benzodiazepines who metabolize long-acting benzodiazepines more slowly and vice versa. The changes are most notable with long acting benzodiazepines as these are prone to significant accumulation in such individuals and can lead to withdrawal symptoms.Script error: No such module "Unsubst". For example, the equivalent dose of diazepam in an elderly individual on lorazepam may be half of what would be expected in a younger individual.[7][8] Equivalent doses of benzodiazepines differ as much as 20 fold.[9][10][11]

Pharmacokinetic properties of various benzodiazepines

Equivalency data in the table below is taken from the Ashton "Benzodiazepine Equivalence Table".[4][12][13][14]

Drug Name Common Trade NamesTemplate:Efn Year Approved

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Typical Oral Dosage Formulations

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Approx. Equivalent Oral Dose to 10 mg DiazepamTemplate:Efn <templatestyles src="Nobold/styles.css"/>(mg) Peak Onset of Action

<templatestyles src="Nobold/styles.css"/>(hours)

Elimination Half-life of Active Metabolite <templatestyles src="Nobold/styles.css"/>(hours) Primary Therapeutic Use
Adinazolam Deracyn Template:Maybe 1–2 3 anxiolytic, antidepressant
Alprazolam Xanax, Helex, Xanor, Trankimazin, Onax, Alprox, Misar, Restyl, Solanax, Tafil, Neurol, Frontin, Kalma, Ksalol, Farmapram 1981 0.25, 0.5, 1, 2 0.5 1–3[15] 11-13 [10–20][15] anxiolytic, antidepressant[16]
BentazepamTemplate:Efn Thiadipona 25 1–3 2–4 anxiolytic
Bretazenil[17] 2.5 anxiolytic, anticonvulsant
Bromazepam Lexotanil, Lexotan, Lexilium, Lectopam, Lexaurin, Lexatin, Bromam 1981 1.5, 3, 6 6 1–5 20–40 anxiolytic,

hypnotic, muscle relaxant

Bromazolam Template:Maybe 2 , 4 2 anxiolytic
BrotizolamTemplate:Efn Lendormin, Dormex, Sintonal, Noctilan 0.25 0.5 0.5–2 4–5 hypnotic
Camazepam Albego, Limpidon 40[18] 1–3 6–11 anxiolytic
Chlordiazepoxide Librium, Risolid, Elenium 1960 5, 10, 25 25 1.5–6 36–200 anxiolytic
Cinazepam Levana 0.5, 1, 2 2–4 60 hypnotic, anxiolytic
Cinolazepam Gerodorm 40 0.5–2 9 hypnotic
Clobazam Onfi, Frisium, Urbanol 2011 5, 10, 20 20 1–5 8–60 anxiolytic, anticonvulsant
Clonazepam Rivatril, Rivotril, Klonopin, Iktorivil, Paxam 1975 0.5, 1, 2 0.5-1 1–5 19.5–50 anticonvulsant, anxiolytic
Clonazolam Template:Maybe 0.25, 0.5 0.2 0.5-1 3-4[19] hypnotic, anticonvulsant
Clorazepate Tranxene, Tranxilium 1972 3.75, 5, 7.5 15 Variable 32–152 anxiolytic, anticonvulsant
ClotiazepamTemplate:Efn Veratran, Clozan, Rize 5, 10 10 1–3 4 anxiolytic
Cloxazolam Cloxam, Sepazon, Olcadil 1, 2, 4 1.5[18] 2–5 55–77[18] anxiolytic, anticonvulsant
Delorazepam Dadumir 0.5, 1, 2 1-1.5 1–2 79<[20] anxiolytic, amnesic
DeschloroetizolamTemplate:Efn Template:Maybe 1, 2 4 anxiolytic
Diazepam Antenex, Apaurin, Apzepam, Apozepam, Diazepan, Hexalid, Normabel, Pax, Stesolid, Stedon, Tranquirit, Valium, Vival, Valaxona 1963 2, 5, 10 10 1–1.5 32–205 anxiolytic, anticonvulsant, muscle relaxant, amnesic
Diclazepam[21] Template:Maybe 1, 2 2 1.5–3 42 anxiolytic, muscle relaxant
Estazolam ProSom, Nuctalon 1990 1, 2 2[18] 3–5 10–24 hypnotic, anxiolytic
Ethylbromazolam Template:Maybe 4 (approx. half as potent as bromazolam) anxiolytic
Ethyl carfluzepate Not approved 2 1–5 11–24 hypnotic
EtizolamTemplate:Efn Etilaam, Etizest, Pasaden, Depas Template:Maybe 1 2 1–3 5-7 anxiolytic, muscle relaxant, anticonvulsant
Ethyl loflazepate Victan, Meilax, Ronlax 2[18] 2.5–3 73–119 anxiolytic
Flualprazolam Template:Maybe 0.5, 1 0.25 1-2 12-22 anxiolytic, hypnotic
Flubromazepam[22] Templex Template:Maybe 4, 8, 12 4 1.5–8 100–220 anxiolytic, hypnotic, amnesic, muscle relaxant, anticonvulsant
Flubromazolam Remnon Template:Maybe 0.25, 0.5 0.075 0.5-5 10-20[23] hypnotic
FluclotizolamTemplate:Efn Template:Maybe 0.25-0.5 anxiolytic
Flunitrazepam Rohypnol, Hipnosedon, Vulbegal, Fluscand, Flunipam, Ronal, Rohydorm, Hypnodorm 1972 1, 2 1.5 0.5–3 18–200 hypnotic
Flunitrazolam Template:Maybe 0.25, 0.5 0.1 0.5-1 5-13 hypnotic
Flurazepam Dalmadorm, Dalmane, Fluzepam 1970 30 20-25 1–1.5 40–250 hypnotic
Flutazolam Coreminal 4 10 1-3 47-100 hypnotic
Flutemazepam Template:Maybe 1 0.5-5 8-20 hypnotic, anxiolytic, anticonvulsant, muscle relaxant[24]
Flutoprazepam Restas 1984 1, 2 2.5 0.5–9 87[25] hypnotic, anticonvulsant, muscle relaxant
Halazepam Alapryl, Paxipam 1981 20, 40 40 3–6 15-35 [30-100] anxiolytic
Ketazolam Anxon, Sedotime 1980 15, 30, 45 20 2.5–6 30-100 [36-200] anxiolytic
Loprazolam Dormonoct, Havlane 1983 1, 2 1.5 2–5 6–20[26] hypnotic
Lorazepam Ativan, Orfidal, Lorenin, Lorsilan, Temesta, Tavor, Lorabenz 1977 0.5, 1, 2, 2.5 1 2–4 10–20 anxiolytic, anticonvulsant, hypnotic, muscle relaxant[27][14][28]
Lormetazepam Loramet, Noctamid, Pronoctan 1984 1, 2 1.5 0.5–2 10-12 hypnotic, anxiolytic
Meclonazepam Template:Maybe 6 anxiolytic
Medazepam Nobrium, Ansilan, Mezapam, Rudotel, Raporan 10 10 4-8 36–200 anxiolytic
MetizolamTemplate:Efn Template:Maybe 1, 2, 4 2–4 12 anxiolytic
Mexazolam Melex, Sedoxil 0.5, 1 1–2 anxiolytic
Midazolam Dormicum, Flormidal, Versed, Hypnovel, Dormonid 1985 7.5, 15 10 (oral)

4 (IV)

0.5–1 1.8-6 hypnotic, anticonvulsant
Nifoxipam Template:Maybe 0.5, 1, 2 hypnotic
Nimetazepam Erimin, Lavol 1984 5 2.5-5 0.5–3 14–30 hypnotic
Nitemazepam Template:Maybe 2 0.5-5 10-27 hypnotic, anticonvulsant
Nitrazepam Mogadon, Alodorm, Pacisyn, Dumolid, Nitrazadon 1965 5, 10 5 0.5–7 17–48 hypnotic, anticonvulsant
Nitrazolam Template:Maybe 0.5, 1 hypnotic
Nordazepam Madar, Stilny 5, 7.5, 15 10-15 30–150 anxiolytic
Norflurazepam Template:Maybe 5 47-100 hypnotic
Oxazepam Seresta, Serax, Serenid, Serepax, Sobril, Oxabenz, Oxapax, Oxascand, Ox-Pam, Opamox, Alepam, Medopam, Murelax, Noripam, Purata 1965 10, 15, 30, 50 30 3–4 4–11 anxiolytic
Phenazepam Phenazepam, Phenzitat Template:Maybe 1.5–4 60 anxiolytic, anticonvulsant
Pinazepam Domar, Duna 5, 10 40–100 anxiolytic
Prazepam Demetrin, Lysanxia, Prazene, Centrax 1976 10, 20, 30 15-20 2–6 36–200 anxiolytic
Premazepam Not approved 15 2–6 10–13 anxiolytic
Pyrazolam Template:Maybe 0.25, 0.5, 1 1–1.5 16–18[29] anxiolytic, amnesic
Quazepam Doral, Quiedorm 1985 15 20 1–5 39–120 hypnotic
Rilmazafone Rhythmy 11 hypnotic
Temazepam Restoril, Normison, Euhypnos, Temaze, Tenox 1981 10, 20 15-20 0.5–3 4–11 hypnotic, anxiolytic, muscle relaxant
Tetrazepam Myolastan, Clinoxam, Epsipam, Musaril 50 1–3 3–26 muscle relaxant, anxiolytic
Triazolam Halcion, Rilamir, Notison, Somese 1980 0.125, 0.25 0.5 0.5–2 2 hypnotic
Drug Name Common Trade Names Year Approved Typical Dosages of Oral Tablets

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Approx. Equivalent Oral Dose to 10 mg Diazepam <templatestyles src="Nobold/styles.css"/>(mg) Peak onset of action <templatestyles src="Nobold/styles.css"/>(hours) Elimination Half-life of Active Metabolite <templatestyles src="Nobold/styles.css"/>(hours) Primary Therapeutic Use

Atypical benzodiazepine receptor ligands

Drug Name Common Trade Names Year approved (US FDA) Elimination Half-life of Active Metabolite <templatestyles src="Nobold/styles.css"/>(hours) Primary Therapeutic Use
DMCM anxiogenic, convulsant
FlumazenilTemplate:Efn Anexate, Lanexat, Mazicon, Romazicon 1 antidote
Eszopiclone§ Lunesta 2004 6 hypnotic
Zaleplon§ Sonata, Starnoc 1999 1 hypnotic
Zolpidem§ Ambien, Nytamel, Sanval, Stilnoct, Stilnox, Sublinox (Canada), Xolnox, Zoldem, Zolnod 1992 2.6 hypnotic
Zopiclone§ Imovane, Rhovane, Ximovan; Zileze; Zimoclone; Zimovane; Zopitan; Zorclone, Zopiklone 4–6 hypnotic

Template:Notelist

Controversy

In 2015 the UK's House of Commons attempted to get a two to four week limit mandate for prescribing benzodiazepines to replace the two to four week benzodiazepine prescribing guidelines, which are merely recommended.[30]

Binding data and structure-activity relationship

File:Benzodiazépines en France.jpg
A variety of Benzodiazepines along with their molecular structure.

A large number of benzodiazepine derivatives have been synthesised and their structure-activity relationships explored in detail.[31][32][33][34] This chart contains binding data for benzodiazepines and related drugs investigated by Roche up to the late 1990s (though in some cases the compounds were originally synthesised by other companies such as Takeda or Upjohn).[35][36][37][38][39][40] Other benzodiazepines are also listed for comparison purposes,[41][42][43] but it does not however include binding data for;

While binding or activity data are available for most of these compounds also, the assay conditions vary between sources, meaning that in many cases the values are not suitable for a direct comparison. Many older sources used animal measures of activity (i.e. sedation or anticonvulsant activity) but did not measure in vitro binding to benzodiazepine receptors.[49][50] See for instance Table 2 vs Table 11 in the Chem Rev paper, Table 2 lists in vitro pIC50 values matching those below, while Table 11 has pEC50 values derived from in vivo assays in mice, which show the same activity trends but cannot be compared directly, and includes data for compounds such as diclazepam and flubromazepam which are not available in the main data set.

Also note;

  • IC50 / pIC50 values represent binding affinity only and do not reflect efficacy or pharmacokinetics, and some compounds listed are GABAA antagonists rather than agonists (e.g. flumazenil).
  • Low IC50 or high pIC50 values indicate tighter binding (pIC50 of 8.0 = IC50 of 10nM, pIC50 of 9.0 = IC50 of 1nM, etc.)
  • These are non subtype selective IC50 values averaged across all GABAA receptor subtypes, so subtype selective compounds with strong binding at one subtype but weak at others will appear unusually weak due to averaging of binding values (see e.g. CL-218,872)
  • indicates a predicted value from in silico modelling.[51]
  • Finally, note that the benzodiazepine core is a privileged scaffold, which has been used to derive drugs with diverse activity that is not limited to the GABAA modulatory action of the classical benzodiazepines,[52] such as devazepide and tifluadom, however these have not been included in the list below. 2,3-benzodiazepines such as tofisopam are also not listed, as these act primarily as AMPA receptor modulators, and are inactive at GABAA receptors.

Table

See also

References

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  16. Ashton Manual
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  33. Edinoff AN, Nix CA, Odisho AS, Babin CP, Derouen AG, Lutfallah SC, Cornett EM, Murnane KS, Kaye AM, Kaye AD. Novel Designer Benzodiazepines: Comprehensive Review of Evolving Clinical and Adverse Effects. Neurol Int. 2022 Aug 22;14(3):648-663. Script error: No such module "CS1 identifiers". Template:Catalog lookup link
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  51. Catalani V, Floresta G, Botha M, Corkery JM, Guirguis A, Vento A, Abbate V, Schifano F. In silico studies on recreational drugs: 3D quantitative structure activity relationship prediction of classified and de novo designer benzodiazepines. Chem Biol Drug Des. 2023 Jan;101(1):40-51. Script error: No such module "CS1 identifiers". Template:Catalog lookup link
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Further reading

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