B019
盐酸酚苄明 盐酸盐
≥97%, powder
别名:
N-(2-氯乙基)-N-(1-甲基-2-苯氧乙基)苄胺 盐酸盐
质量水平
方案
≥97%
表单
powder
颜色
white
溶解性
H2O: slightly soluble
alcohol: soluble
propylene glycol: soluble
创始人
Wellspring
储存温度
2-8°C
SMILES字符串
Cl[H].CC(COc1ccccc1)N(CCCl)Cc2ccccc2
InChI
1S/C18H22ClNO.ClH/c1-16(15-21-18-10-6-3-7-11-18)20(13-12-19)14-17-8-4-2-5-9-17;/h2-11,16H,12-15H2,1H3;1H
InChI key
VBCPVIWPDJVHAN-UHFFFAOYSA-N
基因信息
human ... ADRA1A(148), ADRA1B(147), ADRA1D(146), ADRA2A(150), ADRA2B(151), ADRA2C(152)
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生化/生理作用
钙调蛋白拮抗剂；α-肾上腺素受体拮抗剂。
特点和优势
该化合物由Wellspring开发。要浏览其他药物开发化合物和批准的药物/候选药物列表，单击此处。
这种化合物是ADME毒性研究的特色产品。点击此处发现更多特色ADME毒性产品。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。
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Carc. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Is dexmedetomidine the agent of choice in the resection of pheochromocytoma?
Harsha V Polavarapu et al.
The American surgeon, 78(3), E127-E128 (2012-04-25)
Yu Zhu et al.
Endocrine, 38(2), 254-259 (2010-11-04)
The objective of this article is to evaluate the efficacy of Doxazosin Mesylate Controlled Release Tablets for preoperative treatment of patients with pheochromocytoma. Between 2003 and 2008, 67 patients with confirmed diagnoses of pheochromocytoma were enrolled in this study. According
Chandra Srinivasan et al.
Congenital heart disease, 4(5), 329-337 (2009-09-11)
In the past decade, many advances in the care of patients undergoing the Norwood procedure (NP) have been reported, but management remains nonstandardized at many institutions. We studied the impact of a standardized management protocol for neonates undergoing NP. Care
Anouk Scholten et al.
The Journal of clinical endocrinology and metabolism, 98(2), 581-591 (2013-01-04)
Pheochromocytoma crisis is a feared and potentially lethal complication of pheochromocytoma. We sought to determine the best treatment strategy for pheochromocytoma crisis patients and hypothesized that emergency resection is not indicated. Retrospective cohort study (1993-2011); literature review (1944-2011). Tertiary referral
David J Unett et al.
The Journal of pharmacology and experimental therapeutics, 347(3), 645-659 (2013-09-21)
The kinetics of drug-receptor interactions can profoundly influence in vivo and in vitro pharmacology. In vitro, the potencies of slowly associating agonists may be underestimated in assays capturing transient signaling events. When divergent receptor-mediated signaling pathways are evaluated using combinations
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