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Merck
CN

G110

胍那苄 乙酸盐

α2 adrenoceptor agonist, powder

别名:

1-(2,6-二氯亚苄基氨基)胍 乙酸盐, WY-8678

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关于此项目

经验公式（希尔记法）:
C8H8Cl2N4 · C2H4O2
化学文摘社编号:
23256-50-0
分子量:
291.13
NACRES:
NA.77
PubChem Substance ID:
24277775
UNSPSC Code:
12352200
EC Number:
245-534-7
MDL number:
MFCD00153801

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产品名称

胍那苄 乙酸盐, powder

InChI key

MCSPBPXATWBACD-GAYQJXMFSA-N

InChI

1S/C8H8Cl2N4.C2H4O2/c9-6-2-1-3-7(10)5(6)4-13-14-8(11)12;1-2(3)4/h1-4H,(H4,11,12,14);1H3,(H,3,4)/b13-4+;

SMILES string

CC(O)=O.NC(=N)N\N=C\c1c(Cl)cccc1Cl

form

powder

color

white

solubility

H2O: 10 mg/mL
alcohol: 50 mg/mL

originator

Wyeth

Quality Level

200

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

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相关类别

Biochem/physiol Actions

中枢作用的α2 肾上腺素能受体激动剂；I2 咪唑啉结合位点配体；抗高血压活性。

Features and Benefits

《受体分类和信号转导》手册的 α2-肾上腺素受体 以及 咪唑啉结合位点 页面有该化合物的介绍。想要浏览手册的其他页面， 请单击此处。
该化合物由 Wyeth 开发 。要浏览其他制药公司开发的化合物列表批准的药物/候选药物的列表， 点击这里 。
这种化合物是神经科学研究的特色产品。点击此处发现更多特色神经科学产品。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。

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000474835
0000474835
0000362746
0000362745
0000327220

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Fabienne Gug et al.
Bioconjugate chemistry, 21(2), 279-288 (2010-01-23)
The synthesis of affinity matrices for 6-aminophenanthridine (6AP) and 2,6-dichlorobenzylidenaminoguanidine (Guanabenz, GA), two unrelated prion inhibitors, is described. In both cases, the same simple spacer, epsilon-aminocaproylaminopentanol, was introduced by a Mitsunobu reaction and the choice of the anchoring position of
Pavel Tsaytler et al.
Science (New York, N.Y.), 332(6025), 91-94 (2011-03-10)
Many biological processes are regulated through the selective dephosphorylation of proteins. Protein serine-threonine phosphatases are assembled from catalytic subunits bound to diverse regulatory subunits that provide substrate specificity and subcellular localization. We describe a small molecule, guanabenz, that bound to
Pavel Tsaytler et al.
The FEBS journal, 280(2), 766-770 (2012-02-22)
Selective and reversible phosphorylation is one of the most common post-translational modifications of proteins. Although kinase inhibitors are popular in drug development programmes, selective pharmacological manipulation of phosphatase activity has been challenging to achieve. We review recent advances in the
Suzana Dos Reis et al.
Biochimie, 93(6), 1047-1054 (2011-03-15)
The ribosome, the protein synthesis machinery of the cell, has also been implicated in protein folding. This activity resides within the domain V of the main RNA component of the large subunit of the ribosome. It has been shown that
B Holmes et al.
Drugs, 26(3), 212-229 (1983-09-01)
Guanabenz is an orally active central alpha 2-adrenoceptor agonist. Its antihypertensive action is thought to result from a decrease in sympathetic outflow from the brain to the peripheral circulatory system as a result of stimulation of central alpha 2-adrenoceptors. In
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