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Epinastine-13C-d3 (hydrobromide) Sale

(Synonyms: WAL801-13C,d3 hydrobromide) 目录号 : GC47299

A neuropeptide with diverse biological activities

Epinastine-13C-d3 (hydrobromide) Chemical Structure

规格 价格 库存 购买数量
1 mg
¥6,150.00
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Sample solution is provided at 25 µL, 10mM.

Description

Epinastine-13C-d3 is intended for use as an internal standard for the quantification of epinastine by GC- or LC-MS. Epinastine is a histamine H1 receptor antagonist (Kiapps = 1.41 and 1.62 nM using guinea pig cerebellar and lung membranes, respectively) and mast cell stabilizer.1,2 It inhibits IgE-induced histamine, TNF-α, and IL-10 secretion in human cord blood stem cell-derived mast cells (CBMCs) when used at a concentration of 0.1 μg/ml.2 Epinastine inhibits histamine-induced cutaneous vascular permeability in rats and bronchoconstriction in anesthetized guinea pigs (ID50s = 5 and 0.1 mg/kg, respectively).3 It inhibits dye leakage into the conjunctiva in a rat model of passive anaphylaxis reaction-induced vascular hyperpermeability of the conjunctiva (ID50 = 9.7 mg/kg, p.o.).4 Topical administration of formulations containing epinastine (0.05% three times per day) reduces lid edema, tearing, and redness, as well as the number of neutrophils and eosinophils in the lid fornix, in a mouse model of atopic conjunctivitis.2 Formulations containing epinastine have been used in the prevention of itching associated with allergic conjunctivitis.

1.Ter Laak, A.M., DonnÉ-Op den Kelder, G.M., Bast, A., et al.Is there a difference in the affinity of histamine H1 receptor antagonists for CNS and peripheral receptors• An in vitro studyEur. J. Pharmacol.232(2-3)199-205(1993) 2.Galatowicz, G., Ajayi, Y., Stern, M.E., et al.Ocular anti-allergic compounds selectively inhibit human mast cell cytokines in vitro and conjunctival cell infiltration in vivoClin. Exp. Allergy37(11)1648-1656(2007) 3.Matsushita, K., Nobutoshi, A., and Aritake, K.Pharmacological studies on the novel antiallergic drug HQL-79: II. Elucidation of mechanisms for antiallergic and antiasthmatic effectsJpn. J. Pharmacol.78(1)11-22(1998) 4.Tamura, T., Sato, H., Miki, I., et al.Effects of orally administered olopatadine hydrochloride on the ocular allergic reaction in ratsAllergol. Int.52(2)77-83(2003)

化学性质

Cas No. N/A SDF
别名 WAL801-13C,d3 hydrobromide
Canonical SMILES NC1=N[13C]([2H])([2H])C2([2H])C(C=CC=C3)=C3CC(C=CC=C4)=C4N21.Br
分子式 C15[13C]H12D3N3.HBr 分子量 334.2
溶解度 DMSO: soluble,Water: soluble 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.9922 mL 14.9611 mL 29.9222 mL
5 mM 0.5984 mL 2.9922 mL 5.9844 mL
10 mM 0.2992 mL 1.4961 mL 2.9922 mL
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