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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC36760 Ambroxol Ambroxol is a metabolite of Bromhexine that stimulates mucociliary action and clears the air passages in the respiratory tract. It is usually administered as the hydrochloride.
DC36762 Abbott 36581 Butamirate, particularly Butamirate citrate, is a cough suppressant that works by acting centrally through the receptors in the brainstem. It has a very beneficial effect, because it reduces the resistance in the airways by inhibiting bronchospasm and anti-inflammatory effect.
DC36763 Phostriecin Phostriecin, also known as Sultriecin, is an antifungal and antitumor antibiotic from Streptomyces roseiscleroticus.
DC36764 Carbutamide Carbutamide is a sulfonylurea antidiabetic agent with similar actions and uses to chlorpropamide.
DC36765 Niceritrol Niceritrol is an ester of nicotinic acid that lowers cholesterol and triglycerides in total plasma and in the VLD- and LD-lipoprotein fractions.
DC36766 Xenalipin Xenalipin is a hypolipidemic that reduces blood cholesterol and triglycerides in rats.
DC36767 Methisazone Methisazone is an antiviral agent effective against pox viruses.
DC36768 BW245C BW245C has potent platelet anti-aggregating actions following parenteral or oral administration which makes this hydantoin a potentially-useful anti-thrombotic prostaglandin analogue.
DC36769 Phenobarbital Phenobarbital is a barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. Phenobarbital is discontinued.
DC36770 Carazolol Carazolol is a beta1/beta2 adrenoceptor antagonist of high potency used in the treatment of hypertension. Its affinity for the beta 3-adrenoceptor was determined in Chinese hamster ovary cells transfected with the gene of the human or the murine beta 3-adrenoceptor. Carazolol is recognized with a nanomolar affinity, which positions it among the best ligands for beta 3-adrenoceptors.
DC36771 Cefapirin Cefapirin is an antibiotic effective against gram-negative and gram-positive organisms.
DC36772 Ocinaplon Ocinaplon appears to be a well-tolerated and effective treatment for GAD. It produces a rapid onset of anxiolytic action absent the side effects (e.g., dizziness, sedation) typically reported following anxiolytic doses of benzodiazepines.
DC36773 Leucovorin Leucovorin is the active metabolite of folic acid. Leucovorin is used principally as its calcium salt as an antidote to folic acid antagonists which block the conversion of folic acid to folinic acid.
DC36774 Paramethasone Paramethasone is a glucocorticoid with the general properties of corticosteroids. It has been used by mouth in the treatment of all conditions in which corticosteroid therapy is indicated except adrenal-deficiency states for which its lack of sodium-retaining properties makes it less suitable than Hydrocortisone with supplementary Fludrocortisone.
DC36775 Curcumenol Curcumenol is a sesquiterpene isolated from Curcuma zedoaria is known to possess a variety of health and medicinal values which includes neuroprotection, anti-inflammatory, anti-tumor and hepatoprotective activities.
DC36776 Cynaropicrin Cynaropicrin is the first plant natural product with in vivo activity against Trypanosoma brucei.
DC36777 Cyclobendazole Cyclobendazole is an antihelmintic; benzimidazole derivative related to mebendazole.
DC36778 Cyheptamide Cyheptamide is an anticonvulsant.
DC36779 Alminoprofen Alminoprofen is a nonsteroidal anti-inflammatory agent that was found to significantly suppress passive anaphylactic bronchoconstrictions at 30 mg/kg given intraduodenally, while ibuprofen did not at the same doses.
DC36780 Levcromakalim Levcromakalim, also known as Lemakalim, is an anti-asthmatic, antihypertensive, and potassium-ATP channel opener.
DC36781 Oxethazaine Oxethazaine is a surface anesthetic used mainly orally in chronic gastritis & heartburn to analgize the gastric mucosa.
DC36782 Spiroxatrine Spiroxatrine is a potent dopamine antagonist that most likely functions as an agonist at the 5-HT1A receptor. This compound is similar to buspirone in that it has a prominent dopamine antagonist component and has been found to produce greater anxiolytic effects when combined with buspirone.
DC36783 Esmolol Esmolol is a short acting hyperselective β-adrenergic blocker effective in blunting adrenergic response to several perioperative stimuli and so it might interfere in the effect of the anesthetic drugs on the brain. Esmolol is effective not only in attenuating intraoperative hemodynamic changes related to sympathetic overdrive but also in minimizing significant propofol and sevoflurane requirements without compromising the hemodynamic status.
DC36784 Piribedil Piribedil is a dopamine D2 agonist. It is used in the treatment of Parkinson disease, particularly for alleviation of tremor. It has also been used for circulatory disorders and in other applications as a D2 agonist.
DC36785 Syrosingopine Syrosingopine has been found to potentiate the anticancer activity of widely used diabetic drug metformin by sensitizing cancer cells to metformin.
DC36787 Chlorhexidine Chlorhexidine is a disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque.
DC36788 Norgestrel Norgestrel is a synthetic progestational agent with actions similar to those of PROGESTERONE. This racemic or (±)-form has about half the potency of the levo form (LEVONORGESTREL). Norgestrel is used as a contraceptive, ovulation inhibitor, and for the control of menstrual disorders and endometriosis.
DC36789 Sulindac sulfone Featured Sulindac sulfone is an mTORC1 pathway inhibitor and a metabolite of Sulindac. Sulindac sulfone inhibits colon cancer cell growth and induces cell cycle arrest. Sulindac sulfone is used in cancer research.
DC36790 Fucosterol Fucosterol has been reported to have antioxidant, antidiabetic, and anti-inflammatory effects. In one study, fucosterol exhibited a protective effect on LPS-induced acute lung injury with a possible mechanism inhibiting NF-κB activation, thereby inhibiting LPS-induced inflammatory response.
DC36791 Fasudil Featured Fasudil, a Rho-kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats.

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