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B4559

BRL 44408 maleate salt

≥98% (HPLC)

Synonym(s):

2-[2H-(1-Methyl-1,3-dihydroisoindole)methyl]-4,5-dihydroimidazole maleate salt

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About This Item

Empirical Formula (Hill Notation):
C17H21N3O4
CAS Number:
Molecular Weight:
331.37
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Pricing and availability is not currently available.
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Quality Level

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

H2O: soluble 15 mg/mL, clear

originator

GlaxoSmithKline

SMILES string

OC(=O)\C=C/C(O)=O.CC1N(CC2=NCCN2)Cc3ccccc13

InChI

1S/C13H17N3.C4H4O4/c1-10-12-5-3-2-4-11(12)8-16(10)9-13-14-6-7-15-13;5-3(6)1-2-4(7)8/h2-5,10H,6-9H2,1H3,(H,14,15);1-2H,(H,5,6)(H,7,8)/b;2-1-

InChI key

DDIQGSUEJOOQQQ-BTJKTKAUSA-N

Biochem/physiol Actions

BRL 44408 maleate is a selective α2A-adrenoceptor antagonist.

Features and Benefits

This compound is featured on the α2-Adrenoceptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Legal Information

Sold under agreement from Glaxo­Smith­Kline

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Show Differences

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This Item
P9233M110P5514
assay

≥98% (HPLC)

assay

-

assay

≥98% (HPLC)

assay

-

form

powder

form

powder

form

powder

form

powder

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

solubility

H2O: soluble 15 mg/mL, clear

solubility

DMSO: >10 mg/mL, H2O: >10 mg/mL

solubility

H2O: >3 mg/mL, clear (warmed)

solubility

-

color

white to beige

color

-

color

white to dark brown

color

-

originator

GlaxoSmithKline

originator

Servier

originator

-

originator

Watson


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Shawquia Young et al.
Basic & clinical pharmacology & toxicology, 107(2), 690-697 (2010-04-01)
Previously, we reported that antinociceptive synergism of a 5-HT(3)/alpha(2)-adrenoceptor ligand MD-354 (m-chlorophenylguanidine) and clonidine combination occurs, in part, through a 5-HT(3) receptor antagonist mechanism. In the present investigation, a possible role for alpha(2)-adrenoceptors was examined. Mechanistic studies using yohimbine (a
Mu-huo Ji et al.
Cytokine, 60(3), 639-645 (2012-09-11)
To investigate the effects of α2A-adrenoreceptor blockade on acute lung injury (ALI) and high mobility group box-1 protein (HMGB1) expression in a rat model of sepsis. Sepsis was induced in male rats by cecal ligation and puncture (CLP). Thirty adult
Junta Imaki et al.
Neuroscience letters, 454(2), 143-147 (2009-05-12)
We examined the effects of JP-1302 (a selective alpha2C antagonist), BRL-44408 (a selective alpha2A antagonist) and yohimbine (a non-selective alpha2 antagonist) on haloperidol-induced bradykinesia and catalepsy in mice to elucidate the role of alpha2 adrenoceptor subtypes in modifying extrapyramidal motor



Global Trade Item Number

SKUGTIN
B4559-10MG04061833429785
B4559-50MG04061833429808

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