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Merck
CN

E4250

(−)-肾上腺素

≥99% (HPLC), powder, adrenoceptor agonist

别名:

(−)-肾上腺素, (R)-(−)-3,4-二羟基-α-（甲基氨甲基）苯甲醇, L-肾上腺素

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关于此项目

线性分子式:
(HO)2C6H3CH(OH)CH2NHCH3
化学文摘社编号:
51-43-4
分子量:
183.20
Beilstein:
2368277
EC 号:
200-098-7
MDL编号:
MFCD00002204
UNSPSC代码:
12352200
PubChem化学物质编号:
24894545
NACRES:
NA.77

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产品名称

(−)-肾上腺素,

mp

215 °C (dec.) (lit.)

储存温度

2-8°C

SMILES字符串

CNC[C@H](O)c1ccc(O)c(O)c1

InChI

1S/C9H13NO3/c1-10-5-9(13)6-2-3-7(11)8(12)4-6/h2-4,9-13H,5H2,1H3/t9-/m0/s1

InChI key

UCTWMZQNUQWSLP-VIFPVBQESA-N

基因信息

human ... ADRA1A(148), ADRA1B(147), ADRA1D(146), ADRA2A(150), ADRA2B(151), ADRA2C(152), ADRB1(153), ADRB2(154), ADRB3(155)
rat ... Adra1a(29412), Adra2a(25083), Adrb1(24925), Adrb2(24176), Drd1a(24316), Drd2(24318)

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生化/生理作用

肾上腺素受体激动剂。

特点和优势

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-肾上腺素受体和β-肾上腺素受体页面上进行了描述。想要浏览手册的其他页面， 请单击此处。

制备说明

本品仅微溶于水。其他信息源说明它可溶于DMSO(2 mg/mL)。经检测，本品在0.5 M HCl中的溶解度为50 mg/mL。该储液浓度可用缓冲液或培养基进一步稀释至需要的终浓度。培养基一般具有缓冲性，因此不会影响最终的pH。化合物仍留在溶液中。

象形图

Skull and crossbones
GHS06

警示用语：

Danger

危险声明

H301 + H331,H310

危险分类

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

涉药品监管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN7568
BCCK4340
BCCJ3640
BCCG9470
BCCD2065

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