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Toremifene

Toremifene is an oral selective estrogen receptor modulator which helps oppose the actions of estrogen in the body. It is used to treat breast cancer. It works by blocking the activity of estrogen in the breast. This may stop the growth of some breast tumors that need estrogen to grow.

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Totarol

Totarol is a naturally produced phenolic diterpene that is bioactive as (+)-totarol. It was first isolated by McDowell and Esterfield from the heartwood of Podocarpus totara, a yew tree found in New Zealand. Recent studies have confirmed (+)-totarol’s unique antimicrobial and therapeutic properties. Consequently, (+)-totarol is a promising candidate for a new source of drugs and has been the goal of numerous syntheses.

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Trabectedin

Trabectedin is an anti-tumor drug. It is approved for use in Europe, Russia and South Korea for the treatment of advanced soft tissue sarcoma. It is also undergoing clinical trials for the treatment of breast, prostate, and paediatric sarcomas.

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Tramadol

Tramadol is a narcotic analgesic proposed for severe pain. It may be habituating.Tramadol and its O-desmethyl metabolite (M1) are selective, weak OP3-receptor agonists.

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Tramadol Hydrochloride

Tramadol Hydrochloride is a centrally acting opioid analgesic, used in treating moderate to severe pain.It inhibits reuptake of serotonin and norepinephrine in central nervous system.

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Tranexamic Acid

Tranexamic acid is a synthetic derivative of the amino acid lysine. It is used to treat or prevent excessive blood loss during surgery and in various other medical conditions. It is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin, by binding to specific sites of both plasminogen and plasmin, a molecule responsible for the degradation of fibrin. Tranexamic acid is frequently used in surgeries with high risk of blood loss such as cardiac, liver, vascular and large orthopedic procedures. Its oral form is now being evaluated for use in outpatient conditions involving heavy bleeding. Tranexamic acid competitively inhibits activation of plasminogen (via binding to the kringle domain), thereby reducing conversion of plasminogen to plasmin. Tranexamic acid also directly inhibits plasmin activity, but higher doses are required than are needed to reduce plasmin formation.

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Trans-1-(4-hydroxycyclohexyl)-4-(4-Fluorophenyl)-5-(2-Methoxypy-rimidin-4-yl)Imidazole

Trans-1-(4-hydroxycyclohexyl)-4-(4-Fluorophenyl)-5-(2-Methoxypy-rimidin-4-yl)Imidazole is used in pharma applications. It reduces inflammatory cytokine production and is neuroprotective following oral administration in vivo.

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Transdermal Peptide LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Transdermal Peptide. More information please visit the website: http://www.creative-peptides.com/product/transdermal-peptide-item-gr2118-32547.html

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Trastuzumab

Trastuzumab is a monoclonal antibody that interferes with the HER2/neu receptor. Its main use is to treat certain breast cancers.Trastuzumab binds to the HER2 (or c-erbB2) proto-oncogene, an EGF receptor-like protein found on 20-30% of breast cancer cells. The binding leads to antibody mediated (complement mediated) killing of the HER2 positive cells.

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Trazodone

Trazodone is an antidepressant of the serotonin antagonist and reuptake inhibitor class. It is a phenylpiperazine compound. It also has anxiolytic, and hypnotic effects. It has considerably less prominent anticholinergic and sexual side effects than most of the tricyclic antidepressants.

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