Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H25N3O2S2 |
| Molecular Weight | 391.551 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CN1C2=C(SC3=C1C=C(C=C3)S(=O)(=O)N(C)C)C=CC=C2)N(C)C
InChI
InChIKey=VWNWVCJGUMZDIU-UHFFFAOYSA-N
InChI=1S/C19H25N3O2S2/c1-14(20(2)3)13-22-16-8-6-7-9-18(16)25-19-11-10-15(12-17(19)22)26(23,24)21(4)5/h6-12,14H,13H2,1-5H3
| Molecular Formula | C19H25N3O2S2 |
| Molecular Weight | 391.551 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionSources: http://www.mufel.net/plm05/6816.htmCurator's Comment: description was created based on several sources, including, https://www.jstage.jst.go.jp/article/gnam1977/3/2/3_113/_pdf, http://www.ncbi.nlm.nih.gov/pubmed/8564192
Sources: http://www.mufel.net/plm05/6816.htm
Curator's Comment: description was created based on several sources, including, https://www.jstage.jst.go.jp/article/gnam1977/3/2/3_113/_pdf, http://www.ncbi.nlm.nih.gov/pubmed/8564192
Fonzine (also known as dimetotiazine) is an analgesics and anti-inflammatory agent marketed in Japan and Europe under the name Migristene and indicated for the treatment of migraine and headaches secondary to other disease. Fonzine exerts its activity by inhibiting serotonin and histamine H1 receptors.
CNS Activity
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2096904 |
|||
Target ID: P35367 Gene ID: 3269.0 Gene Symbol: HRH1 Target Organism: Homo sapiens (Human) Sources: http://www.ncbi.nlm.nih.gov/pubmed/8564192 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: http://www.mufel.net/plm05/6816.htm |
Primary | MIGRISTENE Approved UseProphylactic and curative treatment of migraine and headaches secondary other diseases. |
||
| Primary | MIGRISTENE Approved UseProphylactic and curative treatment of migraine and headaches secondary other diseases. |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Determination of isothipendyl or dimethothiazine with their sulphoxides using third- and fourth-derivatives spectroscopy on a diode-array spectrophotometer. | 1990-07-01 |
|
| [Clinical use of dimetotiazine (8599RP)]. | 1967-12-10 |
|
| [Resorption, excretion and biotransformation of 3-dimethylsulfamido-10-(2-dimethylaminopropyl)-phenothiazine (Dimetotiazine) in the rabbit and dog]. | 1967-09-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://www.mufel.net/plm05/6816.htm
Take 20-80 mg during the first day (2-4 tablets) and then - 40 mg/day (2 tablets) up to 3 months.
Route of Administration:
Oral
| Substance Class |
Chemical
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| Record UNII |
1FTA475ZDB
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Validated (UNII)
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NCI_THESAURUS |
C66885
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WHO-VATC |
QN02CX05
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WHO-ATC |
N02CX05
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DIMETOTIAZINE
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100000082666
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1235
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7456-24-8
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50138
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C80770
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3089
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m5528
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DB08967
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2034
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1FTA475ZDB
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CHEMBL346977
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231-229-6
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SUB07182MIG
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DTXSID6023076
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
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ACTIVE MOIETY |