I5627
异丙肾上腺素 盐酸盐
≥98.5% (TLC), powder, β-adrenoceptor agonist
别名:
(±)-异丙肾上腺素 盐酸盐, 1-(3′,4′-二羟基苯基)-2-异丙基氨基乙醇 盐酸盐, N-异丙基-DL-去甲肾上腺素 盐酸盐
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选择尺寸
关于此项目
经验公式（希尔记法）:
C11H17NO3 · HCl
化学文摘社编号:
分子量:
247.72
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
200-089-8
MDL number:
Beilstein/REAXYS Number:
3917363
产品名称
异丙肾上腺素 盐酸盐,
InChI key
IROWCYIEJAOFOW-UHFFFAOYSA-N
InChI
1S/C11H17NO3.ClH/c1-7(2)12-6-11(15)8-3-4-9(13)10(14)5-8;/h3-5,7,11-15H,6H2,1-2H3;1H
SMILES string
Cl.CC(C)NCC(O)c1ccc(O)c(O)c1
mp
165-175 °C (dec.) (lit.)
originator
Sanofi Aventis
Quality Level
Gene Information
human ... ADRB1(153), ADRB2(154), ADRB3(155)
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Biochem/physiol Actions
β-肾上腺素受体激活剂；增加胞质cAMP。
Features and Benefits
该化合物是由Sanofi Aventis研发。想要浏览其他由制药公司开发的化合物以及已批准物/候选药物清单， 请单击此处。
Other Notes
仅供研究使用
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Na Tian et al.
Diabetes, 69(7), 1355-1367 (2020-04-17)
Obesity has recently become a prevalent health threat worldwide. Although emerging evidence has suggested a strong link between the pentose phosphate pathway (PPP) and obesity, the role of transketolase (TKT), an enzyme in the nonoxidative branch of the PPP that
Aaron M Ring et al.
Nature, 502(7472), 575-579 (2013-09-24)
G-protein-coupled receptors (GPCRs) are integral membrane proteins that have an essential role in human physiology, yet the molecular processes through which they bind to their endogenous agonists and activate effector proteins remain poorly understood. So far, it has not been
Eric M Jones et al.
eLife, 9 (2020-10-22)
The >800 human G protein-coupled receptors (GPCRs) are responsible for transducing diverse chemical stimuli to alter cell state- and are the largest class of drug targets. Their myriad structural conformations and various modes of signaling make it challenging to understand
Michael Schwarzl et al.
Critical care medicine, 41(12), e401-e410 (2013-08-22)
We tested whether mild hypothermia impacts on circulatory and respiratory dysfunction during experimental endotoxemia. Randomized controlled prospective experimental study. Large animal facility, Medical University of Graz, Austria. Thirteen anesthetized and mechanically ventilated pigs. Lipopolysaccharide was administered for 4 hours. With
Jiao Li et al.
PloS one, 8(3), e58334-e58334 (2013-03-28)
Here we investigate how ß-adrenergic stimulation of the heart alters regulation of ryanodine receptors (RyRs) by intracellular Ca(2+) and Mg(2+) and the role of these changes in SR Ca(2+) release. RyRs were isolated from rat hearts, perfused in a Langendorff
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