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Benzodiazepine designer drug
Nifoxipam Legal status
5-(2-fluorophenyl)-3-hydroxy-7-nitro-2,3-dihydro-1H -1,4-benzodiazepin-2-one
CAS Number PubChem CID ChemSpider UNII CompTox Dashboard (EPA ) Formula C 15 H 10 F N 3 O 4 Molar mass 315.260 g·mol−1 3D model (JSmol )
O=C1C(O)N=C(C2=CC=CC=C2F)C3=CC([N+]([O-])=O)=CC=C3N1
InChI=1S/C15H10FN3O4/c16-11-4-2-1-3-9(11)13-10-7-8(19(22)23)5-6-12(10)17-14(20)15(21)18-13/h1-7,15,21H,(H,17,20)
Key:UHFIFTRHLBAWGY-UHFFFAOYSA-N
Nifoxipam (3-hydroxydesmethylflunitrazepam , DP 370 ) is a benzodiazepine that is a minor metabolite of flunitrazepam and has been sold online as a designer drug .[ 1] [ 2] [ 3] [ 4] [ 5] [ 6] [ 7] [ 8] [ 9]
Nifoxipam produces strong tranquillising and sleep-prolonging effects and has much lower toxicity compared to lormetazepam and flunitrazepam in mice.[ 1]
^ a b EP 0158267 , Posselt K, Wagener HH, Gruber K,, "Pharmaceutical composition containing 5-(2-fluorophenyl)-1,3-dihydro-3-hydroxy-7-nitro- or 5-(2-fluorophenyl)-1,3-dihydro-3-hydroxy-1-methyl-7-nitro-2H-1,4-benzodiazepin-2-one and process for their preparation", published 16 October 1985, assigned to Dolorgiet Beteiligungs-GmbH
^ "Nifoxipam" . New Synthetic Drugs Database. Archived from the original on 2016-11-01. Retrieved 2016-07-08 .
^ Kilicarslan T, Haining RL, Rettie AE, Busto U, Tyndale RF, Sellers EM (April 2001). "Flunitrazepam metabolism by cytochrome P450S 2C19 and 3A4" . Drug Metabolism and Disposition . 29 (4 Pt 1): 460–5. PMID 11259331 .
^ Moosmann B, King LA, Auwärter V (June 2015). "Designer benzodiazepines: A new challenge" . World Psychiatry . 14 (2): 248. doi :10.1002/wps.20236 . PMC 4471986 . PMID 26043347 .
^ Kevin Flemen (August 2015). "Drug Facts - Newer Unregulated Drugs" (PDF) . KFx. Retrieved 15 August 2015 .
^ "Nifoxipam" . WEDINOS.
^ Meyer MR, Bergstrand MP, Helander A, Beck O (May 2016). "Identification of main human urinary metabolites of the designer nitrobenzodiazepines clonazolam, meclonazepam, and nifoxipam by nano-liquid chromatography-high-resolution mass spectrometry for drug testing purposes". Analytical and Bioanalytical Chemistry . 408 (13): 3571–91. doi :10.1007/s00216-016-9439-6 . PMID 27071765 . S2CID 25831532 .
^ Pettersson Bergstrand M, Helander A, Hansson T, Beck O (April 2017). "Detectability of designer benzodiazepines in CEDIA, EMIT II Plus, HEIA, and KIMS II immunochemical screening assays". Drug Testing and Analysis . 9 (4): 640–645. doi :10.1002/dta.2003 . PMID 27366870 .
^ Katselou M, Papoutsis I, Nikolaou P, Spiliopoulou C, Athanaselis S (2016). "Metabolites replace the parent drug in the drug arena. The cases of fonazepam and nifoxipam" . Forensic Toxicology . 35 (1): 1–10. doi :10.1007/s11419-016-0338-5 . PMC 5214877 . PMID 28127407 .
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AA-29504
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DS2
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Terpenoids (e.g., borneol )
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Positive modulators: Alcohols (e.g., brometone , chlorobutanol (chloretone) , ethanol (alcohol) , tert -butanol (2M2P) , tribromoethanol , trichloroethanol , trifluoroethanol )
Alkylbenzene sulfonate
Anandamide
Barbiturates (e.g., pentobarbital , sodium thiopental )
Chlormethiazole
D12-116
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RU-5135
Sinomenine
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Thiocolchicoside
Tutin
Negative modulators: Amiloride
Benzodiazepines (e.g., bromazepam , clonazepam , diazepam , flunitrazepam , flurazepam )
Corymine
Cyanotriphenylborate
Daidzein
Dihydropyridines (e.g., nicardipine , nifedipine , nitrendipine )
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Ginkgo constituents (e.g., bilobalide , ginkgolides (e.g., ginkgolide A , ginkgolide B , ginkgolide C , ginkgolide J , ginkgolide M ))
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NBQX
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GlyT1 Tooltip Glycine transporter 1 GlyT2 Tooltip Glycine transporter 2