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Levodropropizine(DF-526)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Levodropropizine(DF-526)图片
CAS NO:99291-25-5
规格:≥98%
包装与价格:
包装价格(元)
25mg询价
50mg询价
100mg询价
250mg询价
500mg询价
1g询价
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理化性质和储存条件
Molecular Weight (MW)236.31
FormulaC13H20N2O2
CAS No.99291-25-5
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 47 mg/mL (198.9 mM)
Water: 15 mg/mL (63.5 mM)
Ethanol: 47 mg/mL (198.9 mM)
Other info

Chemical Name: (S)-3-(4-phenylpiperazin-1-yl)propane-1,2-diol

InChi Key: PTVWPYVOOKLBCG-ZDUSSCGKSA-N

InChi Code: InChI=1S/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2/t13-/m0/s1

SMILES Code: OC[C@@H](O)CN1CCN(C2=CC=CC=C2)CC1

Synonyms

(S)-(-)-Dropropizine; DF-526; Levodropropizine; DF 526; DF526; Levotuss

实验参考方法
In Vitro

In vitro activity: Levodropropizine has affinity for H1-histaminic and alpha-adrenergic receptors.

In VivoLevodropropizine has weaker central sedative effects than the racemate and it does not induce physical dependence in rats. Levodropropizine (15 mg/kg, i.v.) reduces both the duration of apnoea and the response of the C-fibre to phenylbiguanide. The LVDP-induced inhibition of the C-fibre response to PBG is on average 50% in pulmonary and 25% in non-pulmonary fibres. Levodropropizine is shown to have good antitussive activity in anaesthetized guinea-pigs and rabbits. Levodropropizine (i.v.) is 1/10 to 1/20 as active as codeine and comparable to dropropizine on mechanically and electrically induced coughing in rabbits and guinea-pigs. Levodropropizine (orally) is comparable with those of both dropropizine and codeine against coughing induced by irritant aerosols. Levodropropizine (40 μg/50 μL i.c.v.) does not prevent electrically-induced cough, while Codeine (5 μg/50 μl i.c.v.) markedly prevents coughing in guinea-pigs. Levodropropizine has a peripheral site of action which is related to sensory neuropeptides. Levodropropizine (10 mg/kg, 50 mg/kg and 200 mg/kg) reduces in a dose-dependent manner the extravasation of Evans blue dye evoked by capsaicin in the rat trachea. Levodropropizine (200 mg/kg) inhibits also substance P-evoked extravasation, whereas it does not affect the extravasation evoked by platelet activating factor.
Animal modelRats
Formulation & Dosage15 mg/kg, 10 mg/kg, 50 mg/kg and 200 mg/kg; i.v.
References

Arzneimittelforschung. 1988 Aug;38(8):1144-50; Br J Pharmacol. 1996 Mar;117(5):853-8.

 
 
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