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Merck

M105

Sigma-Aldrich

美索曲明 水合物

≥97% (NMR), solid

别名:

N,N′-bis[6-[[(2-甲氧基苯基)甲基]氨基]己基] -1,8-辛烷二胺 四盐酸盐 水合物, 美索曲明 四盐酸盐 水合物

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About This Item

经验公式(希尔记法):
C36H62N4O2 · 4HCl · xH2O
分子量:
728.75 (anhydrous basis)
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.32

品質等級

化驗

≥97% (NMR)

形狀

solid

顏色

white

溶解度

H2O: >20 mg/mL

儲存溫度

2-8°C

SMILES 字串

O.Cl.Cl.Cl.Cl.COc1ccccc1CNCCCCCCNCCCCCCCCNCCCCCCNCc2ccccc2OC.COc3ccccc3CNCCCCCCNCCCCCCCCNCCCCCCNCc4ccccc4OC

InChI

1S/2C36H62N4O2.4ClH.H2O/c2*1-41-35-23-13-11-21-33(35)31-39-29-19-9-7-17-27-37-25-15-5-3-4-6-16-26-38-28-18-8-10-20-30-40-32-34-22-12-14-24-36(34)42-2;;;;;/h2*11-14,21-24,37-40H,3-10,15-20,25-32H2,1-2H3;4*1H;1H2

InChI 密鑰

XIIINYPADNNZHA-UHFFFAOYSA-N

基因資訊

human ... CHRM2(1129)

一般說明

甲辛胺(N, N′-双[6-[[((2-甲氧基苯基)-甲基]己基] -1,8-辛烷]二胺)是聚亚甲基四胺的衍生物。

應用

水合甲辛胺:
  • 作为毒蕈碱受体 2 的拮抗剂已用于。
  • 作为测试分子,检查其对 HGPS(Hutchinson-Gilford 早衰综合症)iPS(诱导多能性)衍生的间充质干细胞的过早成骨分化的影响。

生化/生理作用

美索曲明是 nM 浓度下的选择性 M2 毒蕈碱受体拮抗剂。在 mM 浓度下,美索曲明直接抑制 G 蛋白的高亲和力 GTPase 活性。在食管肌肉中,M2 受体拮抗剂美索曲明可降低乙酰胆碱介导的钙和花生四烯酸释放的增加。在背外侧纹状体两侧注入美索曲明,使得认知功能受损的老年大鼠记忆力显著增强。美索曲明在毒蕈碱受体分类中起着至关重要的作用。
美索曲明是 nM 浓度下的选择性 M2 毒蕈碱受体拮抗剂。在 mM 浓度下,美索曲明直接抑制 G 蛋白的高亲和力 GTPase 活性。M2 受体拮抗剂美索曲明可降低钙和花生四烯酸释放的增加,但 M3 受体拮抗剂对氟-六氢-硅杂-地芬尼多不能。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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