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Merck

F6145

Supelco

Fenspirid -hydrochlorid

analytical standard, for drug analysis

Synonym(e):

8-(2-Phenylethyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-on -hydrochlorid

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About This Item

Empirische Formel (Hill-System):
C15H20N2O2 · HCl
CAS-Nummer:
Molekulargewicht:
296.79
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:

Qualität

analytical standard

Qualitätsniveau

Assay

>99% (TLC)

Form

powder

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Farbe

white

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

SMILES String

Cl.O=C1NCC2(CCN(CCc3ccccc3)CC2)O1

InChI

1S/C15H20N2O2.ClH/c18-14-16-12-15(19-14)7-10-17(11-8-15)9-6-13-4-2-1-3-5-13;/h1-5H,6-12H2,(H,16,18);1H

InChIKey

FIKFLLIUPUVONI-UHFFFAOYSA-N

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem./physiol. Wirkung

Bronchodilator with anti-inflammatory properties. Inhibits mucus secretion and reduces the release of tachykinins at a prejunctional level by its anti-muscarinic action. It also may be an antagonist at α adrenergic and H1 histamine receptors.
Fenspiride hydrochloride possesses anti-allergic and anti-bronchoconstrictive properties. It is used as a drug to treat inflammatory conditions of the upper and lower respiratory tracts. Experimental studies state that fenspiride has an ability to reduce the development of myringosclerosis, possibly by restricting the formation of oxygen-derived free radicals.
Bronchospasmolytikum mit enzündungshemmender Wirkung. Inhibiert die Schleimsekretion und verringert die Freisetzung von Tachykininen (Neurokininen) durch seine antimuskarinische Wirkung auf einem prejunktionalen Level. Es ist möglicherweise auch ein Antagonist von a Adrenozeptoren und H1 Histaminrezeptoren.

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Analysenzertifikate (COA)

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J Cortijo et al.
European journal of pharmacology, 341(1), 79-86 (1998-03-07)
We have investigated the role of human bronchial cyclic nucleotide phosphodiesterases in the effects of fenspiride, a drug endowed with bronchodilator and anti-inflammatory properties. Functional studies on human isolated bronchi showed that fenspiride (10(-6)-3 x 10(-3) M, 30 min) induced
J C Féray et al.
Biochemical pharmacology, 54(2), 293-297 (1997-07-15)
Fenspiride inhibits the calcium signal evoked by the inflammatory peptide formyl-Met-Leu-Phe (fMLP) in peritoneal macrophages, but at concentrations (approximately 1 mM) far above the therapeutic range (approximately 1 microM). Here, in rat alveolar macrophages, high fenspiride concentrations (1 mM) were
Inhibition of the development of myringosclerosis by local administration of fenspiride, an anti-inflammatory drug.
Mattsson C and Hellstrom S
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated With the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, 254(9-10), 425-429 (1997)
F Quartulli et al.
European journal of pharmacology, 348(2-3), 297-304 (1998-07-04)
Using the human lung epithelial WI26VA4 cell line, we investigated the capacity of fenspiride, an anti-inflammatory drug with anti-bronchoconstrictor properties, to interfere with histamine-induced intracellular Ca2+ increase and eicosanoid formation. Histamine and a histamine H1 receptor agonist elicited a rapid

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