Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H18ClFN2O3 |
| Molecular Weight | 376.809 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCN1C2=CC=C(Cl)C=C2C3(OCCN3CC1=O)C4=CC=CC=C4F
InChI
InChIKey=WMFSSTNVXWNLKI-UHFFFAOYSA-N
InChI=1S/C19H18ClFN2O3/c20-13-5-6-17-15(11-13)19(14-3-1-2-4-16(14)21)22(8-10-26-19)12-18(25)23(17)7-9-24/h1-6,11,24H,7-10,12H2
| Molecular Formula | C19H18ClFN2O3 |
| Molecular Weight | 376.809 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionSources: http://med.sawai.co.jp/file/pr22_1083.pdf
Sources: http://med.sawai.co.jp/file/pr22_1083.pdf
Flutazolam is a benzodiazepine derivative developed in Japan by Mitsui. The drug is marketed under the name Coreminal and used for the treatment of gastrointestinal disorders. The mechanism of flutazolam action is due to activation of GABA-A receptors as it has affinity to the benzodiazepine binding sites.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2109243 Sources: http://med.sawai.co.jp/file/pr22_1083.pdf |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Palliative | COREMINAL Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.014 μg/mL |
12 mg single, oral dose: 12 mg route of administration: Oral experiment type: SINGLE co-administered: |
FLUTAZOLAM serum | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.068 μg × h/mL |
12 mg single, oral dose: 12 mg route of administration: Oral experiment type: SINGLE co-administered: |
FLUTAZOLAM serum | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Detectability of designer benzodiazepines in CEDIA, EMIT II Plus, HEIA, and KIMS II immunochemical screening assays. | 2017-04 |
|
| Simultaneous determination of twelve benzodiazepines in human serum using a new reversed-phase chromatographic column on a 2-microns porous microspherical silica gel. | 1996-06-28 |
|
| [Studies on the clinical significance concerning the changes in serum pepsinogen-I and gastrin levels in aged patients with chronic gastritis]. | 1988-03 |
|
| [The behavior of 1,4-benzodiazepine drugs in acidic media. IX. Effect of hydrolyzate of flutazolam on the central nervous system]. | 1987-10 |
|
| The behavior of 1,4-benzodiazepine drugs in acidic media. V. Kinetics of hydrolysis of flutazolam and haloxazolam in aqueous solution. | 1986-01 |
|
| [Psychopharmacological effects of flutazolam (MS-4101) (author's transl)]. | 1978-11 |
Sample Use Guides
In Vivo Use Guide
Sources: http://med.sawai.co.jp/file/pr22_1083.pdf
The usual adult dose is 12 mg administered 3 times/day.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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5G2K7O5D8S
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C1012
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CHEMBL1697836
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m1171
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C65737
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3398
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Flutazolam
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C013367
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DTXSID6023072
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27060-91-9
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
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METABOLITE ACTIVE -> PARENT |
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ACTIVE MOIETY |