All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Glunicate | NCIT_C87632 | [A long-acting nicotinic acid derivative with antilipidemic activity. Glunicate has more prolonged activity on plasma free fatty acids and triglycerides, with longer lasting and more intense activity on plasma cholesterol than nicotinic acid or its derivative, niceritrol. In animal models glunicate showed dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation. These effects were independent of its effects on lowering plasma lipid levels.] |
| Niacin-based Antilipidemic Agent | NCIT_C98151 | [An antilipidemic agent that works through, or mimics, the action of niacin to increase HDL-C levels by blocking hepatic uptake of apolipoprotein A-1 and decreasing HDL clearance. The use of free niacin is limited by its side effects of skin flushing (i.e., redness, itching, burning, and paresthesias).] |
| Moxipraquine | NCIT_C87633 | |
| Sitamaquine | NCIT_C73010 | |
| Fenpiverinium | NCIT_C87638 | |
| Flutropium | NCIT_C87639 | |
| Quinocide | NCIT_C73004 | |
| Integration | NCIT_C48038 | [An operation used in calculus whereby the integral of a function is determined.] |
| Artesunate | NCIT_C73005 | [A water-soluble, semi-synthetic derivative of the sesquiterpine lactone artemisinin with anti-malarial, anti-schistosomiasis, antiviral, and potential anti-neoplastic activities. Upon hydrolysis of artesunate's active endoperoxide bridge moiety by liberated heme in parasite-infected red blood cells, reactive oxygen species and carbon-centered radicals form, which have been shown to damage and kill parasitic organisms. Additionally, in vitro studies demonstrate that this agent induces DNA breakage in a dose-dependent manner. Artesunate has also been shown to stimulate cell differentiation, arrest the cell cycle in the G1 and G2/M phases, inhibit cell proliferation, and induce apoptosis through mitochondrial and caspase signaling pathways. Artemisinin is isolated from the plant Artemisia annua.] |
| Spot | NCIT_C48039 | [A mark on a substance or body made by foreign matter; a blot; a place discolored.] |
| Tafenoquine | NCIT_C73006 | |
| Benzetimide | NCIT_C73007 | |
| Marriage | NCIT_C48033 | [The social institution involving legal and/or religious sanction whereby men and women are joined together for the purpose of founding a family unit; the state of being a married couple.] |
| Amopyroquine | NCIT_C73000 | |
| Artemether | NCIT_C73001 | |
| Artemotil | NCIT_C73002 | |
| Operator | NCIT_C48036 | [A person that operates some apparatus or machine.] |
| Pamaquine | NCIT_C73003 | |
| Pyridoxine Hydrochloride | NCIT_C48030 | [The hydrochloride salt form of pyridoxine, a water-soluble vitamin B. Pyridoxine hydrochloride is converted into the active form, pyridoxal 5'-phosphate (PLP), an essential cofactor in many enzymatic activities including synthesis of amino acids, neurotransmitters, and sphingolipids. This vitamin is essential to red blood cell, nervous system, and immune systems functions and helps maintain normal blood glucose levels.] |
| Ziprasidone Hydrochloride | NCIT_C48031 | [The hydrochloride salt form of ziprasidone, a benzothiazolylpiperazine derivative and an atypical antipsychotic agent with an antischizophrenic property. Ziprasidone hydrochloride functions as an antagonist at the dopamine D2 and serotonin 5-HT2A and 5-HT1D receptors, and as an agonist at the 5-HT1A receptor. Ziprasidone hydrochloride also inhibits synaptic reuptake of serotonin and norepinephrine. The mechanism of action by which ziprasidone hydrochloride exerts its antischizophrenic effect is unknown but is potentially mediated through a combination of dopamine D2 and serotonin 5-HT2 antagonism. This agent also has antagonistic activity against histamine H1 and alpha-1-adrenergic receptors.] |