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Merck
CN

P7791

哌唑嗪 盐酸盐

≥99.0% (HPLC), powder, α1-adrenoceptor antagonist

别名:

1-(4-氨基-6,7-二甲氧基-2-喹唑啉基)-4-(2-呋喃甲酰基)哌嗪 盐酸盐, 脉宁平 盐酸盐

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关于此项目

经验公式(希尔记法):
C19H21N5O4 · HCl
化学文摘社编号:
分子量:
419.86
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
242-903-4
MDL number:
Beilstein/REAXYS Number:
4303561
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产品名称

哌唑嗪 盐酸盐, ≥99.0% (HPLC)

InChI key

WFXFYZULCQKPIP-UHFFFAOYSA-N

InChI

1S/C19H21N5O4.ClH/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14;/h3-4,9-11H,5-8H2,1-2H3,(H2,20,21,22);1H

SMILES string

Cl.COc1cc2nc(nc(N)c2cc1OC)N3CCN(CC3)C(=O)c4ccco4

assay

≥99.0% (HPLC)

form

powder

solubility

H2O: 0.5 mg/mL
methanol: 6 mg/mL
dilute aqueous acid: insoluble

Quality Level

Gene Information

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Application

盐酸哌唑嗪已用于:
  • 阻断介导小鼠交感血管收缩的 α1 肾上腺素能受体
  • 作为 α1-肾上腺素受体阻滞剂,大鼠灌胃给药
  • 作为血管扩张剂,与胰岛素一起注入小鼠左心室,评价其对肾功能的影响

Biochem/physiol Actions

外周 α1-肾上腺素能受体拮抗剂;血管扩张剂。哌唑嗪可用于治疗慢性创伤后应激障碍(PTSD)。它通过舒张血管起降血压作用,因此可用于治疗高血压。

Disclaimer

吸湿;光敏感。

Features and Benefits

该化合物在《受体分类和信号转导手册》的α1-肾上腺素受体α2-肾上腺素受体褪黑激素页面上进行了描述。想要浏览手册的其他页面, 请单击此处
这种化合物是 ADME 毒性和神经科学研究的特色产品。发现更多特色 ADME 毒性神经科学产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

General description

哌唑嗪是一种α-肾上腺素能阻滞剂。它被视为一种周围血管舒张抗高血压药物。哌唑嗪是喹唑啉的衍生物。

Packaging

无底玻璃瓶。内含物装在插入的融合锥内。

pictograms

Health hazardExclamation mark

signalword

Warning

Hazard Classifications

Repr. 2 - STOT RE 2 - STOT SE 3

target_organs

Central nervous system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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The authors conducted a 15-week randomized controlled trial of the alpha-1 adrenoreceptor antagonist prazosin for combat trauma nightmares, sleep quality, global function, and overall symptoms in active-duty soldiers with posttraumatic stress disorder (PTSD) returned from combat deployments to Iraq and

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