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Azelaic Acid

Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley.It is industrially produced by the ozonolysis of oleic acid. It is effective against a number of skin conditions.It may be useful as a hair growth stimulant.

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Azelastine

Azelastine is a potent, second-generation, selective, histamine antagonist. Azelastine nasal spray is indicated for the local treatment of the symptoms of seasonal allergic rhinitis and perennial allergic rhinitis, such as rhinorrhea, sneezing and nasal pruritis in adults and children 5 years of age and older. Azelastine eyes drops are indicated for the local treatment of seasonal and perennial allergic conjunctivitis. It is also effective in those patients who previously failed to respond to oral antihistamine therapy. Azelastine alleviates the symptom of nasal congestion to a greater degree than oral anti-histamines, an important observation since this is a particularly bothersome symptom for many rhinitis sufferers, and second-generation anti-histamines have traditionally shown little decongestant activity.

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Azelastine Hydrochloride

Azelastine Hydrochloride is an Histamine H1 Receptor (H1-receptor) antagonist, with antiallergic effects related to histamine antagonism, and further antiallergic and antiinflammatory effects unrelated to H1-receptor binding. It is an activator of NF κB.

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Azelnidipine

Azelnidipine is a dihydropyridine calcium channel blocker. It has a gradual onset and has a long-lasting hypotensive effect, with little increase in heart rate.

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Azepane

Azepane is a heterocycle. It can be used as intermediate for pharmaceuticals , agrochemcials, zeolites, dyes , inks, rubber chemicals, textile chemicals and corrosion inhibitors.

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Azidomorphine

Azidomorphine is an opiate analogue that is a derivative of morphine, where the 7,8 double bond has been saturated and the 6-hydroxy group has been replaced by an azide group. It binds with high affinity to the mu opioid receptor. It has similar effects to other opioid agonists including analgesia, sedation and respiratory depression. However its addiction liability has been found to be slightly lower than that of morphine in animal studies.

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Azilsartan Medoxomil

Azilsartan Medoxomil is a prodrug, is hydrolyzed to azilsartan in the gastrointestinal tract during absorption. It is specifically indicated for the treatment of hypertension, alone or in combination with other antihypertensive agents.

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Azimilide

Azimilide is a class ΙΙΙ antiarrhythmic drug. The agents from this heterogeneous group have an effect on the repolarization, they prolong the duration of the action potential and the refractory period. Also they slow down the spontaneous discharge frequency of automatic pacemakers by depressing the slope of diastolic depolarization. They shift the threshold towards zero or hyperpolarize the membrane potential. Although each agent has its own properties and will have thus a different function.

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Azithromycin Dihydrate

Azithromycin Dihydrate is a semi-synthetic macrolide antibiotic that is related to Erythromycin A. Azithromycin Dihydrate exhibits cross-resistance to erythromycin-resistant, gram-positive strains and resistance to most strains of enterococcus faecalis and methicillin-resistant staphylococcus aureus. It is primarily used to treat respiratory tract and skin infections.

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Aztreonam

Aztreonam is a synthetic monocyclic beta-lactam antibiotic, with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum. It is resistant to some beta-lactamases, but is inactivated by extended-spectrum beta-lactamases.

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