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Bremazocine is a κ-opioid receptor agonist related to pentazocine. It has potency and long-lasting analgesic and diuretic effects.


Brofaromine is a reversible inhibitor of monoamine oxidase A primarily useful in the treatment of depression and anxiety. It also has serotonin reuptake inhibitory properties and its dual pharmacologic effects offer promise in the treatment of a wide spectrum of depressed patients while producing less severe anticholinergic side effects in comparison with standard drugs although it is not commercially available and is not being actively researched, possibly due to a lack of financial interest.


Bupivacaine is a local anaesthetic drug belonging to the amino amide group. Bupivacaine is indicated for local anesthesia including infiltration, nerve block, epidural, and intrathecal anesthesia. Bupivacaine often is administered by epidural injection before total hip arthroplasty. It also is commonly injected to surgical wound sites to reduce pain for up to 20 hours after the surgery. Bupivacaine binds to the intracellular portion of sodium channels and blocks sodium influx into nerve cells, which prevents depolarization.

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Butorphanol is a morphinan-type synthetic opioid analgesic. Brand name Stadol was recently discontinued by the manufacturer. It is most closely structurally related to levorphanol. It is available only as butorphanol tartrate in injectable and intranasal spray formulations. It is a commonly used narcotic for pain relief in horses.

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Cabazitaxel is a semi-synthetic derivative of a natural taxoid. It was developed by Sanofi-Aventis and was approved by the U.S. Food and Drug Administration (FDA) for the treatment of hormone-refractory prostate cancer on June 17, 2010. It is a microtubule inhibitor.

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Cadralazine is an antihypertensive of the hydrazine chemical class.

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Cajeput Oil

The cajeput oil is essential oil produced from the leaves and twigs of the Cajeput tree.It is used in perfumery, fragrance, flavor and in Ayurvedic medicine.

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Caloxin 2A1

Caloxin 2A1 is a peptide obtained by screening a random peptide phage display library for binding to the second extracellular domain (residues 401-413) sequence of PM Ca2+ pump isoform 1b. Caloxin 2A1 inhibits Ca2+-Mg2+-ATPase in human erythrocyte leaky ghosts, but it does not affect basal Mg2+-ATPase or Na+-K+-ATPase in the ghosts or Ca2+-Mg2+-ATPase in the skeletal muscle sarcoplasmic reticulum. Caloxin 2A1 also inhibits Ca2+-dependent formation of the 140-kDa acid-stable acylphosphate, which is a partial reaction of this enzyme.


Campesterol is a phytosterol whose chemical structure is similar to that of cholesterol. It is thought to have anti-inflammatory effects. Campesterol was demonstrated that it inhibits several pro-inflammatory and matrix degradation mediators typically involved in osteoarthritis-induced cartilage degradation.


Candesartan is an angiotensin II receptor antagonist used mainly for the treatment of hypertension.

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