β-phenethylamine

3-(TRIFLUOROMETHYL)PHENETHYLAMINE, with CAS No. 52516-30-0, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-(TRIFLUOROMETHYL)PHENETHYLAMINE provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Phosphonomycin (R)-1-phenethylamine salt is a useful organic compound for research related to life sciences. The catalog number is T65395 and the CAS number is 25383-07-7.

Phenibut (Aminophenylbutyric acid) is a central depressant and derivative of the naturally occurring inhibitory neurotransmitter γ-aminobutyric acid (GABA).

Phenethylamine, 3-chloro-alpha,beta-dimethyl- is a bioactive chemical.

Phenibut hydrochloride (3-Amino-4-phenylbutyric acid hydrochloride) is a GABA mimetic that acts as an agonist at GABAB receptors, blocks α2δ subunit-containing voltage-gated calcium channels, stimulates dopamine receptors, and inhibits the actions of β-phenethylamine

N-Phenethylacetamide is an amide derivative of phenethylamine that can be used as a reference standard for quality control and analytical testing, and it can also be employed as an effective antimicrobial agent for use in aquaculture systems.

Tyramine (Uteramine) is an indirect sympathomimetic that occurs naturally in cheese and other foods. Tyramine does not directly activate adrenergic receptors, but it can serve as a substrate for adrenergic uptake systems and MONOAMINE OXIDASE to prolong the actions of adrenergic transmitters. It also provokes transmitter release from adrenergic terminals and may be a neurotransmitter in some invertebrate nervous systems.

3-Methylphenethylamine, with CAS No. 55755-17-4, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-Methylphenethylamine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

N-Methylphenethylamine (NMPEA) hydrochloride is a potent TAAR1 agonist and also functions as a trace amine neuromodulator.

(±)-Amiflamine (2-dimethylphenethylamine) is an inhibitor of reversible MAO-A.

3,4-Dimethoxyphenethylamine is a human endogenous metabolite.

(+)-Benzylphenethylamine is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

Ritodrine hydrochloride (NSC 291565) binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine hydrochloride (NSC 291565) is a phenethylamine derivative with tocolytic activity. Specifically, Ritodrine hydrochloride (NSC 291565) probably activates adenyl cyclase, thereby increasing production of cyclic adenosine monophosphate (cAMP), which in turn enhances the efflux of calcium from vascular smooth muscle cells. A lack of intracellular calcium prevents uterine myometrial contractions. In addition, this agent may directly inactivate myosin light chain kinase, a critical enzyme necessary for the initiation of muscle contractions.

Ritodrine hydrochloride (Standard) is the standard substance of Ritodrine hydrochloride, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Ritodrine hydrochloride (NSC 291565) binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine hydrochloride (NSC 291565) is a phenethylamine derivative with tocolytic activity. Specifically, Ritodrine hydrochloride (NSC 291565) probably activates adenyl cyclase, thereby increasing production of cyclic adenosine monophosphate (cAMP), which in turn enhances the efflux of calcium from vascular smooth muscle cells. A lack of intracellular calcium prevents uterine myometrial contractions. In addition, this agent may directly inactivate myosin light chain kinase, a critical enzyme necessary for the initiation of muscle contractions.