Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H14FN3O |
Molecular Weight | 283.3003 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(C=CC=C1)N2C(=O)C3=CC(N)=CC=C3N=C2CF
InChI
InChIKey=VDOSWXIDETXFET-UHFFFAOYSA-N
InChI=1S/C16H14FN3O/c1-10-4-2-3-5-14(10)20-15(9-17)19-13-7-6-11(18)8-12(13)16(20)21/h2-8H,9,18H2,1H3
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/7109348Curator's Comment: Description was created based on several sources, including https://www.researchgate.net/publication/235333319_Quinazoline_Marketed_drugs_-_A_Review
Sources: http://www.ncbi.nlm.nih.gov/pubmed/7109348
Curator's Comment: Description was created based on several sources, including https://www.researchgate.net/publication/235333319_Quinazoline_Marketed_drugs_-_A_Review
Afloqualone (AFQ) is one of the centrally acting muscle relaxants. It is a quinazolinone family GABAergic drug and is an analogue of methaqualone developed in the 1970s by a team at Tanabe Seiyaku. It has sedative and muscle-relaxant effects resulting from its agonist activity at the β subtype of the GABAa receptor, and has had some clinical use, although it causes photosensitization as a side-effect that can cause skin problems such as dermatitis.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GABA receptor alpha, Beta subtype, Felis catus Sources: http://www.ncbi.nlm.nih.gov/pubmed/7109348 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Sources: http://www.ndrugs.com/?s=arofuto |
Primary | Arofuto Approved UseIndications: muscle hypertonia, spastic paralysis |
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Sources: http://www.ndrugs.com/?s=arofuto |
Primary | Arofuto Approved UseIndications: muscle hypertonia, spastic paralysis |
Sample Use Guides
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/7327456
Afloqualone inhibited spontaneous movements of isolated rabbit atrium and ileum and isolated rat uterus at considerably high concentrations of 10(-6) g/ml or more.
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WIKIPEDIA |
Designer-drugs-Afloqualone
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NCI_THESAURUS |
C29696
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100000087689
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DTXSID5022562
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CO4U2C8ORZ
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SUB05281MIG
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C033541
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CHEMBL2105918
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56287-74-2
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2040
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AFLOQUALONE
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m1445
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C83522
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4831
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ACTIVE MOIETY