Dimetotiazin
10-(2-(Dimethylamino)propyl)-N,N-dimethyl-10H-phenothiazine-2-sulfonamide
Grundinformationen
- CAS
7456-24-8- Standard-SMILES
CC(CN1c2ccccc2Sc2ccc(S(=O)(=O)N(C)C)cc21)N(C)C- InChIKey
VWNWVCJGUMZDIU-UHFFFAOYSA-N- Summenformel
- C19H25N3O2S2
- Durchschnittliche Molmasse
- 391,6 g/mol
- Monoisotopische Masse
- 391,13881904
Überblick
Dimetotiazine is a member of phenothiazines.
Namen und Bezeichner
- Bevorzugter Name
- 10-(2-(Dimethylamino)propyl)-N,N-dimethyl-10H-phenothiazine-2-sulfonamide
- IUPAC
- 10-[2-(dimethylamino)propyl]-N,N-dimethylphenothiazine-2-sulfonamide
- Lokaler Name
- Dimetotiazin
- Englischer Name
- Dimetotiazine
- Summenformel
- C19H25N3O2S2
- Molmasse
- 391.557
Namen und Synonyme
DimetotiazineFONAZINEDimethothiazine7456-24-8DimetotiazinaDimetotiazinum10-(2-(Dimethylamino)propyl)-N,N-dimethylphenothiazine-2-sulfonamide1FTA475ZDBDTXSID6023076Phenothiazine-2-sulfonamide, 10-(2-(dimethylamino)propyl)-N,N-dimethyl-8599 R.P.IL-6302
Weitere Namen anzeigen
8599RPBayer 1483DimethodinBrn 0941549DimetothiazineDimethiotazine
10-[2-(dimethylamino)propyl]-N,N-dimethylphenothiazine-2-sulfonamideDTXCID80307610-[2-(Dimethylamino)propyl]-N,N-dimethyl-10H-phenothiazine-2-sulfonamide10-(2-(Dimethylamino)propyl)-N,N-dimethyl-10H-phenothiazine-2-sulfonamideRefChem:599591N02CX05231-229-6Dimetiotazine
Datenbank-Bezeichner
- CAS
7456-24-8- PubChem CID
- 3089
- DTXSID
DTXSID6023076
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,8
- Polarare Oberfläche (TPSA)
- 77,5 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 6
- Frei drehbare Bindungen
- 5
- Schwere Atome
- 26
- Formalladung
- 0
- Komplexität
- 576
Physikochemische Eigenschaften
- Siedepunkt
- 533.7 · 533.7±60.0 °C(Predicted)
- Dichte
- 1.1822 · 1.1822 (rough estimate)
- Brechungsindex
- 1.656 · 1.6560 (estimate)
- pka
- 8.91 · 8.91±0.50(Predicted)
Chemie und Industrie
Pharmakologische Informationen
ATC Code
N - Nervous system
QN - Nervous system
MeSH Pharmacological Classification
Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood.
Anwendungen
VerwendenSerotonin inhibitor.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Anbieter9 Anbieter
LGM Pharma1-(800)-881-8210 · [email protected]
陕西缔都医药化工有限公司+86-29-87569262 +86-15003564040 · [email protected]
BOC Sciences16314854226; +8616314854226 · [email protected]
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