Ticlopidine HCl

立即咨询

Ticlopidine HCl

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。

CAS NO:

53885-35-1

产品介绍

生物活性

Ticlopidine是一种二磷酸腺苷（ADP）受体抑制剂。它通过阻断ADP受体来改变血小板膜的功能，从而抑制血小板聚集。这防止了糖蛋白IIb/IIIa的构象变化，从而使血小板与血纤蛋白原结合。

化学数据

目录号	A11690
M. Wt	300.25
Formula	C14H14ClNS.HCl
Purity	>99%
Storage	Store lyophilized at -20ºC, keep desiccated. In lyophilized form, the chemical is stable for36 months. In solution, store at -20ºC and use within3 monthsto prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.
CAS No.	53885-35-1
SMILES	C1CN(CC2=C1SC=C2)CC3=CC=CC=C3Cl.Cl

溶解度

In vitro	DMSO	1 mg/mL (3.33 mM)
	Water	3 mg/mL (9.99 mM)
	Ethanol	1 mg/mL (3.33 mM)
<1 mg/ml means slightly soluble or insoluble. Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

储备液配制

Concentration / Solvent Volume / Mass	1 mg	5 mg	10 mg
0.1 mM	33.31 mL	166.53 mL	333.06 mL
0.5 mM	6.66 mL	33.31 mL	66.61 mL
1 mM	3.33 mL	16.65 mL	33.31 mL
5 mM	0.67 mL	3.33 mL	6.66 mL

*The above data is based on the productmolecular weight 300.25. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.