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stx-209

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  • Inhibitors & Agonists
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(R)-baclofen
STX209, Arbaclofen
T635569308-37-8
(R)-baclofen (STX209), a derivative of gamma-aminobutyric acid, is commonly utilized for the treatment of spasticity.
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Baclofen
Lioresal
T10651134-47-0
Baclofen (Lioresal) is a synthetic chlorophenyl-butanoic acid derivative used to treat spasms due to spinal cord damage and multiple sclerosis, muscle-relaxing Baclofen acts as a gamma-aminobutyric acid (GABA) agonist specific for GABA-B receptors. It acts at spinal and supraspinal sites, reducing excitatory transmission.
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Baclofen-d4
TMIJ-03141189938-30-4
Baclofen-d4 is a deuterated compound of Baclofen. Baclofen has a CAS number of 1134-47-0. Baclofen is a synthetic chlorophenyl-butanoic acid derivative used to treat spasms due to spinal cord damage and multiple sclerosis, muscle-relaxing Baclofen acts as a gamma-aminobutyric acid (GABA) agonist specific for GABA-B receptors. It acts at spinal and supraspinal sites, reducing excitatory transmission.
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20 days
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(R)-Baclofen hydrochloride
Arbaclofen hydrochloride
T1730663701-55-3
Arbaclofen hydrochloride, a Gamma-Aminobutyric Acid derivative, is a specific agonist of GABA-B receptors, it is used to treat spasticity, especially that due to spinal cord damage. It acts at spinal and supraspinal sites, generally reduces excitatory tra
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1-2 weeks
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(S)-Baclofen hydrochloride
S(-)-Baclofen hydrochloride, S(-)-Baclofen HCl
T20293663701-56-4
(S)-baclofen (also known as L-baclofen), an enantiomer of baclofen, directly mimics the action of GABA-B receptors. In the treatment of trigeminal neuralgia, L-baclofen demonstrates significantly improved efficacy compared to racemic baclofen.
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Baclofen hydrochloride
4-amino-3-(4-chlorophenyl)butanoic acid hydron chloride
T863028311-31-1
Baclofen hydrochloride (4-amino-3-(4-chlorophenyl)butanoic acid hydron chloride) is a GAMMA-AMINOBUTYRIC ACID derivative that is a specific GABA-B RECEPTORS agonist. It is used in the treatment of MUSCLE SPASTICITY, especially that due to SPINAL CORD INJURIES. Its therapeutic effects result from actions at spinal and supraspinal sites, generally the reduction of excitatory transmission.
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(S)-Baclofen
(L)-Baclofen, (+)-Baclofen
T2096266514-99-6
(S)-Baclofen has effects on excitation in the ascending auditory pathway leading to it a potential reagent for the treatment of hyperactive auditory disorders such as hyperacusis and tinnitus.
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6-8 weeks
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