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Merck

D2531

Sigma-Aldrich

Dextromethorphan -hydrobromid Monohydrat

≥99% (TLC)

Synonym(e):

(9S,13S,14S)-3-Methoxy-17-methylmorphinan -hydrobromid

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About This Item

Empirische Formel (Hill-System):
C18H25NO · HBr · H2O
CAS-Nummer:
Molekulargewicht:
370.32
Beilstein:
6453793
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥99% (TLC)

Form

powder

SMILES String

Br[H].[H]O[H].[H][C@]12CCCC[C@]13CCN(C)[C@H]2Cc4ccc(OC)cc34

InChI

1S/C18H25NO.BrH.H2O/c1-19-10-9-18-8-4-3-5-15(18)17(19)11-13-6-7-14(20-2)12-16(13)18;;/h6-7,12,15,17H,3-5,8-11H2,1-2H3;1H;1H2/t15-,17+,18+;;/m1../s1

InChIKey

STTADZBLEUMJRG-IKNOHUQMSA-N

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Anwendung

Dextromethorphan hydrobromide monohydrate has been used as a substrate for cytochrome P450 2D6 enzyme action, in potassium phosphate buffer for measuring P450 activity and is used in enzyme inhibition studies.

Biochem./physiol. Wirkung

Dextromethorphan hydrobromide is an allosteric antagonist at N-methyl D- aspartate (NMDA)-controlled ion channels and antagonist at voltage-dependent channels. Dextromethorphan hydrobromide is useful in treating dry cough.

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Chronic 2

Lagerklassenschlüssel

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Supelco

PHR1974

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Levallorphan tartrate salt ≥98% (HPLC), powder

Sigma-Aldrich

L121

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Dextrorphan tartrate solution 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

Supelco

D-034

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Montelukast ≥98% (HPLC)

Sigma-Aldrich

SML0101

Montelukast

Furafylline ≥98% (HPLC)

Sigma-Aldrich

F124

Furafylline

The effect of prototypic sigma ligands on the binding of [3H]dextromethorphan to guinea pig brain.
Klein, et al.
Neuroscience Letters, 91, 175-175 (1989)
Dependence on dextromethorphan hydrobromide.
Fleming Philip M
British Medical Journal (Clinical Research ed.), 293(6547), 597-597 (1986)
J M Musacchio et al.
Life sciences, 45(19), 1721-1732 (1989-01-01)
There is increasing evidence that sigma ligands and dextromethorphan (DM) bind to at least one common high-affinity site. DM and other antitussives do not produce psychotomimetic effects. This suggested that sigma ligands may produce their characteristic effects through another site
T Zimmermann et al.
Arzneimittel-Forschung, 45(1), 41-43 (1995-01-01)
The polymorphism of dextromethorphan (CAS 125-71-3) metabolism is dependent on hepatic cytochrom P4502D6 (CYP2D6) activity. The relationship between the CYP2D6 genotype and the dextromethorphan phenotype was studied in 83 healthy unrelated subjects. Genotype was determined by allele-specific polymerase chain reaction
In Vitro Inhibition and Induction of Human Liver Cytochrome P450 Enzymes by Gentiopicroside: Potent Effect on CYP2A6
Deng Y, et al.
Drug Metabolism and Pharmacokinetics, 28(4), 339-344 (2013)

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