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  1. World Encyclopedia
  2. Dimdazenil - Wikipedia
Dimdazenil - Wikipedia
From Wikipedia, the free encyclopedia
(Redirected from EVT-201)
Chemical compound

Pharmaceutical compound
Dimdazenil
Clinical data
Trade namesJunoenil
Other namesEVT-201; EVT201
ATC code
  • N05CD16 (WHO)
Legal status
Legal status
  • Rx in China
Identifiers
IUPAC name
  • 7-Chloro-3-[5-[(dimethylamino)methyl]-1,2,4-oxadiazol-3-yl]-5-methyl-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one
CAS Number
  • 308239-86-3
PubChem CID
  • 9885841
DrugBank
  • DB05721
ChemSpider
  • 8061514
UNII
  • 6J8AF7CLE4
KEGG
  • D13231
ChEMBL
  • ChEMBL5095096
CompTox Dashboard (EPA)
  • DTXSID301032055 Edit this at Wikidata
Chemical and physical data
FormulaC17H17ClN6O2
Molar mass372.81 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • Clc4cccc3n2cnc(c1nc(on1)CN(C)C)c2CN(C(=O)c34)C
InChI
  • InChI=1S/C17H17ClN6O2/c1-22(2)8-13-20-16(21-26-13)15-12-7-23(3)17(25)14-10(18)5-4-6-11(14)24(12)9-19-15/h4-6,9H,7-8H2,1-3H3
  • Key:JCYLWUVDHLVGER-UHFFFAOYSA-N

Dimdazenil, sold under the brand name Junoenil, is a medication used in the treatment of insomnia in China.[1] It is a benzodiazepine derivative and a partial positive allosteric modulator of the GABAA receptor[2] with two- to four-fold higher functional affinity for the α1 subunit relative to the α2, α3, and α5 subunits.

Medical use

[edit]

Dimdazenil shows effectiveness in the treatment of insomnia, but has less intrinsic activity in comparison to currently-marketed benzodiazepines and the Z-drugs;[3] however, it is thought that the lower efficacy may result in fewer side effects, such as motor incoordination.[3] In China, dimdazenil is approved for short-term treatment of insomnia.[4]

History

[edit]

Dimdazenil was originally developed by Roche, based on preclinical data, as a non-sedating anxiolytic, but was found to produce sedation in humans in phase I clinical trials. For this reason, it was subsequently licensed to Evotec, which is now developing it for the treatment of insomnia.[3] By 2007, dimdazenil completed phase II clinical trials for this indication, with positive findings reported.[5] In China, the drug was developed by Zhejiang Jingxin Pharmaceutical.

References

[edit]
  1. ^ Huang Z, Zhan S, Chen C, Zhang R, Zhou Y, He J, et al. (February 2024). "Efficacy and safety of Dimdazenil in adults with insomnia disorder: results from a multicenter, randomized, double-blind, placebo-controlled phase III trials". Sleep. 47 (2). doi:10.1093/sleep/zsad272. PMC 10851846. PMID 37875349.
  2. ^ Guilleminault C (2010). Sleep Medicine. Elsevier Health Sciences. pp. 574–. ISBN 978-1-4377-1836-2.
  3. ^ a b c Monti JM, Pandi-Perumal SR, Möhler H (28 September 2010). GABA and Sleep: Molecular, Functional and Clinical Aspects. Springer Science & Business Media. pp. 50–51. ISBN 978-3-0346-0226-6.
  4. ^ Syed YY (March 2024). "Dimdazenil: First Approval". Drugs. doi:10.1007/s40265-024-02020-9. PMID 38546956.
  5. ^ Plunkett JW (September 2007). Plunkett's Biotech & Genetics Industry Almanac 2008: Biotech & Genetics Industry Market Research, Statistics, Trends & Leading Companies. Plunkett Research, Ltd. pp. 311–. ISBN 978-1-59392-087-6.
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Volatiles/gases
  • Acetone
  • Acetophenone
  • Acetylglycinamide chloral hydrate
  • Aliflurane
  • Benzene
  • Butane
  • Butylene
  • Centalun
  • Chloral
  • Chloral betaine
  • Chloral hydrate
  • Chloroform
  • Cryofluorane
  • Desflurane
  • Dichloralphenazone
  • Dichloromethane
  • Diethyl ether
  • Enflurane
  • Ethyl chloride
  • Ethylene
  • Fluroxene
  • Gasoline
  • Halopropane
  • Halothane
  • Isoflurane
  • Kerosine
  • Methoxyflurane
  • Methoxypropane
  • Nitric oxide
  • Nitrogen
  • Nitrous oxide
  • Norflurane
  • Paraldehyde
  • Propane
  • Propylene
  • Roflurane
  • Sevoflurane
  • Synthane
  • Teflurane
  • Toluene
  • Trichloroethane (methyl chloroform)
  • Trichloroethylene
  • Vinyl ether
Others/unsorted
  • 3-Hydroxybutanal
  • α-EMTBL
  • AA-29504
  • Alogabat
  • Avermectins (e.g., ivermectin)
  • Bromide compounds (e.g., lithium bromide, potassium bromide, sodium bromide)
  • Carbamazepine
  • Chloralose
  • Chlormezanone
  • Clomethiazole
  • Darigabat
  • DEABL
  • Deuterated etifoxine
  • Dihydroergolines (e.g., dihydroergocryptine, dihydroergosine, dihydroergotamine, ergoloid (dihydroergotoxine))
  • DS2
  • Efavirenz
  • Etazepine
  • Etifoxine
  • Fenamates (e.g., flufenamic acid, mefenamic acid, niflumic acid, tolfenamic acid)
  • Fluoxetine
  • Flupirtine
  • Hopantenic acid
  • KRM-II-81
  • Lanthanum
  • Lavender oil
  • Lignans (e.g., 4-O-methylhonokiol, honokiol, magnolol, obovatol)
  • Loreclezole
  • Menthyl isovalerate (validolum)
  • Monastrol
  • Nicotinic acid
  • Nicotinamide
  • Org 25,435
  • Phenytoin
  • Propanidid
  • Retigabine (ezogabine)
  • Safranal
  • Seproxetine
  • Stiripentol
  • Sulfonylalkanes (e.g., sulfonmethane (sulfonal), tetronal, trional)
  • Terpenoids (e.g., borneol)
  • Topiramate
  • Valerian constituents (e.g., isovaleric acid, isovaleramide, valerenic acid, valerenol)
  • Unsorted benzodiazepine site positive modulators: α-Pinene
  • MRK-409 (MK-0343)
  • TCS-1105
  • TCS-1205
See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators
Portal:
  • icon Medicine
Retrieved from "https://teknopedia.ac.id/w/index.php?title=Dimdazenil&oldid=1334054027"
Categories:
  • Chloroarenes
  • Dimethylamino compounds
  • GABAA receptor positive allosteric modulators
  • Hypnotics
  • Imidazobenzodiazepines
  • Oxadiazoles
  • Sedatives
Hidden categories:
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  • Use dmy dates from November 2025
  • Short description is different from Wikidata
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Sunting pranala
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