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Merck
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文件

E4250

Sigma-Aldrich

(−)-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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About This Item

线性分子式:
(HO)2C6H3CH(OH)CH2NHCH3
CAS号:
51-43-4
分子量:
183.20
Beilstein:
2368277
EC號碼:
200-098-7
MDL號碼:
MFCD00002204
分類程式碼代碼:
12352200
PubChem物質ID:
24894545
NACRES:
NA.77

product name

(−)-肾上腺素,

品質等級

200

mp

215 °C (dec.) (lit.)

儲存溫度

2-8°C

SMILES 字串

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 密鑰

UCTWMZQNUQWSLP-VIFPVBQESA-N

基因資訊

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。

特點和優勢

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。

重構

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。

象形圖

Skull and crossbones
GHS06

訊號詞

Danger

危險聲明

H301 + H331,H310

危險分類

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

儲存類別代碼

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

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

分析证书(COA)

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