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AB120325

(R)-Baclofen, GABAB agonist

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(4 Publications)

MW 213.66 Da, Purity >98%. More active enantiomer of selective GABAB agonist (R,S)-Baclofen (ab120149). Soluble in 1 ml water to give specified mM/ml concentration.
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Chemical Structure - (R)-Baclofen, GABAB agonist (AB120325)
  • Chemical Structure

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Chemical Structure - (R)-Baclofen, GABAB agonist (AB120325)

2D chemical structure image of ab120325, (R)-Baclofen, GABAB agonist

Key facts

CAS number

69308-37-8

Purity

>98%

Form

Solid

form

Molecular weight

213.66 Da

Molecular formula

C<sub>1</sub><sub>0</sub>H<sub>1</sub><sub>2</sub>ClNO<sub>2</sub>

PubChem

44602

Nature

Synthetic

Biochemical name

Arbaclofen

Biological description

More active enantiomer of selective GABAB agonist (R,S)-Baclofen (ab120149). Soluble in 1 ml water to give specified mM/ml concentration.

Canonical smiles

C1=CC(=CC=C1C(CC(=O)O)CN)Cl

Isomeric smiles

C1=CC(=CC=C1[C@@H](CC(=O)O)CN)Cl

InChi

InChI=1S/C10H12ClNO2/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14/h1-4,8H,5-6,12H2,(H,13,14)/t8-/m0/s1

InChiKey

KPYSYYIEGFHWSV-QMMMGPOBSA-N

IUPAC Name

(3R)-4-amino-3-(4-chlorophenyl)butanoic acid

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

CYP2D6 also known as Cytochrome P450 2D6 is a highly studied enzyme with diverse roles in drug metabolism. It has a molecular mass of approximately 55 kDa. This enzyme is mainly found in the liver but also shows expression in the brain and other tissues. CYP2D6 is one of the cytochrome P450 proteins which includes CYP2C8 CYP2C9 CYP2C19 and CYP2C12. Another relevant target in this context is the GABA B Receptor 2 also referred to as GABBR2 which partners with GABA B Receptor 1. These receptors are expressed in the central nervous system and are important for GABAergic neurotransmission.
Biological function summary

Enzymes like CYP2D6 play an important role in metabolizing around 25% of prescription drugs which includes the processing of antidepressants antipsychotics and beta-blockers. CYP2D6 functions as part of the cytochrome P450 complex which catalyzes the oxidation of organic substances. The GABA B Receptor 2 and 1 form a heterodimeric complex on neuronal cells which mediate slow synaptic transmission through GABA the primary inhibitory neurotransmitter in the CNS. Compounds such as baclofen a known GABA B agonist interact with these receptors to produce muscle relaxant and antispastic effects. Understanding the baclofen structure and its interaction with receptors helps in drug design and application.

Pathways

CYP2D6 is an important player in the metabolism of xenobiotics affecting the pharmacokinetics of many drugs through the oxidation pathway. It interacts with CYP3A4 in the Phase I metabolism pathway further modulating drug activity and clearance. In the context of neurotransmission pathways the GABA B Receptor 2 along with GABA B Receptor 1 modulates neural excitability and calcium channel activity. These actions link it indirectly to pathways involving neurotransmitter release and receptor signaling playing a role in inhibitory synaptic transmission.

CYP2D6 variations are linked with altered drug metabolism impacting treatment outcomes for psychiatric and cardiovascular diseases. Poor metabolizer phenotypes of CYP2D6 can lead to adverse drug reactions and reduced efficacy. The GABA B Receptor 2 and 1 couple because their imbalance has been linked with neurological disorders such as epilepsy and spasticity. In these disorders baclofen’s role as a GABA B agonist is important for therapeutic interventions highlighting its structure-function relationship in modulating receptor response.

Product protocols

Publications (4)

Recent publications for all applications. Explore the full list and refine your search

eLife 9: PubMed32073397

2020

Presynaptic GABA receptors functionally uncouple somatostatin interneurons from the active hippocampal network.

Applications

Unspecified application

Species

Unspecified reactive species

Sam A Booker,Harumi Harada,Claudio Elgueta,Julia Bank,Marlene Bartos,Akos Kulik,Imre Vida

Physiological reports 5: PubMed28196855

2017

Inactivation of GIRK channels weakens the pre- and postsynaptic inhibitory activity in dorsal raphe neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Nerea Llamosas,Luisa Ugedo,Maria Torrecilla

The Journal of neuroscience : the official journal of the Society for Neuroscience 33:804-13 PubMed23303956

2013

Medial prefrontal cortex inversely regulates toluene-induced changes in markers of synaptic plasticity of mesolimbic dopamine neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Jacob T Beckley,Caitlin E Evins,Hleb Fedarovich,Meghin J Gilstrap,John J Woodward

Molecular pharmacology 79:758-67 PubMed21189269

2010

Effects of the allosteric antagonist 1-(4-chlorophenyl)-3-[3-(6-pyrrolidin-1-ylpyridin-2-yl)phenyl]urea (PSNCBAM-1) on CB1 receptor modulation in the cerebellum.

Applications

Unspecified application

Species

Unspecified reactive species

Xiaowei Wang,James G Horswill,Benjamin J Whalley,Gary J Stephens
View all publications

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