Pharmaceutical Raw Materials Pregabalin Intermediate Treats Epilepsy 148553-50-8 With Safe Pass

Pharmaceutical Raw Materials Pregabalin Intermediate Treats Epilepsy 148553-50-8 With Safe Pass

Abstracto

CASO:148553-50-8
MF:C8H17NO2
MW:159.23
EINECS:200-659-6
Punto de fusion:194-196° C
alpha D23 +10.52° (c = 1.06 in water)
punto de inflamabilidad:9℃
temperatura de almacenamiento. Store at RT
solubility deionized water: ≥10mg/mL
InChIKeyAYXYPKUFHZROOJ-ZETCQYMHSA-N

Descripción

1. Pregabalin is a new anti-epileptic drug, gamma-aminobutyrate structure in its molecular structure, with anticonvulsant effects, and successful development of the company’s treatment of peripheral neuropathic pain, or partial seizures. In December 2008, la Administración de Alimentos y Medicamentos de EE.UU. (FDA) approved Pregabalin (trademark Lyrica) for the treatment of diabetic peripheral neuropathic pain (DPN) and post-heat pain neuralgia (PHN), both of which are the most Common neuropathic pain.
2. Neuropathic pain is one of the most difficult treatments for chronic pain syndrome. It is a major feature of relieving pain, burning, and tingling. There are many nerve pains, diabetes, infections (such as herpes zoster), cancer and AIDS that can cause nerve pain. Acerca de 3% of the population in Europe suffer from neuralgia and torture.

Estanozolol semielaborado de la serie líquida de esteroides

Pregabalina, also known as beta-isobutyl-aminobutyric acid (beta-isobutyl-GABA), is a drug used to treat epilepsy, dolor neuropático, fibromyalgia, and generalized anxiety disorder. Common side effects include: lethargy, confusión, memory impairment, poor coordination, dry mouth, vision problems, and weight gain. Potentially serious side effects include angioedema, drug abuse, and increased risk of suicide.
Pregabalin is primarily excluded from the systemic circulation through renal excretion as an unaltered drug. Pregabalin is mainly excreted in urine (≥98%) . Pregabalin has an average elimination half-life of 6.3 horas. 50% of patients will receive a negative urine sample within 3 dias, and a total of 5 days will be required to obtain a negative urine sample of the maximum urine concentration detected in the subject.
The PGB Rapid Detection Panel (Urine) is a rapid urine screening test that can be performed without the use of an instrument. The test used a monoclonal antibody to selectively detect elevated levels of Prepabatin in the urine. Adjusting the quick test panel (urine) produces a positive result when compared to more than 50μg / ml in urine

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