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Triflunordazepam: Difference between revisions

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{{Short description|Chemical compound}}
{{Drugbox {{Drugbox
| verifiedrevid = 449872408 | verifiedrevid = 451563038
| IUPAC_name = 5-phenyl-7-(trifluoromethyl)-1,3-dihydro-1,4-benzodiazepin-2-one | IUPAC_name = 5-phenyl-7-(trifluoromethyl)-1,3-dihydro-1,4-benzodiazepin-2-one
| image = triflunordazepam.png | image = Triflunordazepam.svg
| width = 180 | width = 222


<!--Clinical data--> <!--Clinical data-->
| tradename = | tradename =
| legal_status = | legal_CA = Schedule IV
| legal_UK = PSA
| legal_DE = NpSG
| legal_status =


<!--Pharmacokinetic data--> <!--Pharmacokinetic data-->
Line 13: Line 17:
| metabolism = | metabolism =
| elimination_half-life = | elimination_half-life =
| excretion = | excretion =


<!--Identifiers--> <!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 2285-16-7 | CAS_number = 2285-16-7
| ATC_prefix = none | ATC_prefix = none
| PubChem = 16795 | PubChem = 16795
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 8CS486VL3D
| ChemSpiderID = 15920
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank_Ref = {{drugbankcite|correct|drugbank}}


<!--Chemical data--> <!--Chemical data-->
| C=16 | H=11 | F=3 | N=2 | O=1 | C=16 | H=11 | F=3 | N=2 | O=1
| molecular_weight = 304.267
| smiles = C1C(=O)NC2=C(C=C(C=C2)C(F)(F)F)C(=N1)C3=CC=CC=C3 | smiles = C1C(=O)NC2=C(C=C(C=C2)C(F)(F)F)C(=N1)C3=CC=CC=C3
| StdInChI = 1S/C16H11F3N2O/c17-16(18,19)11-6-7-13-12(8-11)15(20-9-14(22)21-13)10-4-2-1-3-5-10/h1-8H,9H2,(H,21,22)
| StdInChIKey = UUBMOUNXQFMBQF-UHFFFAOYSA-N
}} }}


'''Ro5-2904''' ('''Triflunordazepam''') is a drug which is a ] derivative with high ] affinity, and has ] effects.<ref>''Archives Internationales de Pharmacodynamie et de Therapie''. (1965). Vol 154, p 131.</ref><ref name="pmid8978853">{{cite journal |author=So SS, Karplus M |title=Genetic neural networks for quantitative structure-activity relationships: improvements and application of benzodiazepine affinity for benzodiazepine/GABAA receptors |journal=Journal of Medicinal Chemistry |volume=39 |issue=26 |pages=5246–56 |year=1996 |month=December |pmid=8978853 |doi=10.1021/jm960536o |url=}}</ref> '''Triflunordazepam''' (also known as '''Ro5-2904''')<ref>{{cite patent | country = DE | number = 1136709 }}</ref> is a drug which is a ] derivative with high ] affinity, and has ] effects.<ref>{{cite journal | title = Ro5-2904 | journal = Archives Internationales de Pharmacodynamie et de Thérapie | date = 1965 | volume = 154 | pages = 131 }}</ref><ref name="pmid8978853">{{cite journal | vauthors = So SS, Karplus M | title = Genetic neural networks for quantitative structure-activity relationships: improvements and application of benzodiazepine affinity for benzodiazepine/GABAA receptors | journal = Journal of Medicinal Chemistry | volume = 39 | issue = 26 | pages = 5246–56 | date = December 1996 | pmid = 8978853 | doi = 10.1021/jm960536o }}</ref>


==See also== == See also ==
*]
*] *]
*]


==References== == References ==
{{reflist}}
<references/>


{{Benzodiazepines}} {{Benzodiazepines}}
{{GABAAR PAMs}}


] ]
] ]
]
] ]
]



{{sedative-stub}} {{sedative-stub}}

Latest revision as of 19:42, 20 December 2023

Chemical compound Pharmaceutical compound
Triflunordazepam
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
IUPAC name
  • 5-phenyl-7-(trifluoromethyl)-1,3-dihydro-1,4-benzodiazepin-2-one
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H11F3N2O
Molar mass304.272 g·mol
3D model (JSmol)
SMILES
  • C1C(=O)NC2=C(C=C(C=C2)C(F)(F)F)C(=N1)C3=CC=CC=C3
InChI
  • InChI=1S/C16H11F3N2O/c17-16(18,19)11-6-7-13-12(8-11)15(20-9-14(22)21-13)10-4-2-1-3-5-10/h1-8H,9H2,(H,21,22)
  • Key:UUBMOUNXQFMBQF-UHFFFAOYSA-N
  (verify)

Triflunordazepam (also known as Ro5-2904) is a drug which is a benzodiazepine derivative with high GABAA receptor affinity, and has anticonvulsant effects.

See also

References

  1. DE 1136709 
  2. "Ro5-2904". Archives Internationales de Pharmacodynamie et de Thérapie. 154: 131. 1965.
  3. So SS, Karplus M (December 1996). "Genetic neural networks for quantitative structure-activity relationships: improvements and application of benzodiazepine affinity for benzodiazepine/GABAA receptors". Journal of Medicinal Chemistry. 39 (26): 5246–56. doi:10.1021/jm960536o. PMID 8978853.
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See also: Receptor/signaling modulatorsGABA receptor modulatorsGABA metabolism/transport modulators
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