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Results for "

salivation

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    11
    TargetMol | Inhibitors_Agonists
  • Natural Products
    2
    TargetMol | Natural_Products
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    TargetMol | Recombinant_Protein
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Anethole trithione
Anetholtrithion
T1285532-11-6
Anethole trithione (Anetholtrithion) is a bile secretion-stimulating drug that restores salivation and relieves the discomfort of dry mouth in chemotherapy-induced xerostomia.
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TargetMol | Citations Cited
Flonicamid
UNII-9500W2Z53J, N-(cyanomethyl)-4-(trifluoromethyl)nicotinamide
T20713158062-67-0
Flonicamid (N-(cyanomethyl)-4-(trifluoromethyl)nicotinamide), a pyridinecarboxamide insecticide, inhibits aphid (M. persicae) salivation and sap ingestion during feeding on Japanese radish leaves. It induces toxicity in the aphid species A. gossypii, L. erysimi, R. padi, and S. graminum and rats.
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4-6 weeks
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Glycopyrrolate
Glycopyrrolate bromide, Gastrodyn, Robinul, Glycopyrronium bromide
T2387596-51-0
Glycopyrrolate (Glycopyrrolate bromide) is a muscarinic antagonist used as an antispasmodic, in some disorders of the gastrointestinal tract, and to reduce salivation with some anesthetics.
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λ-Cyhalothrin
lambda-Cyhalothrin, Karate, Icon
T2779491465-08-6
λ-Cyhalothrin (Icon) is a type II synthetic pyrethroid insecticide featuring a high-efficiency, broad-spectrum formula with an α-cyano group. It is employed across various applications for controlling a wide array of pests. As a neurotoxin, λ-Cyhalothrin acts on sodium channels in neuron membranes within the central nervous system.
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Cinperene
R5046
T1361514796-24-8
Cinperene is an atropine-like compound that can block pilocarpine-induced salivation and lacrimation.
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6-8 weeks
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Cevimeline hydrochloride hemihydrate
T2390153504-70-2
Cevimeline hydrochloride hemihydrate is a novel muscarinic receptor agonist, used as a candidate therapeutic drug for xerostomia in Sjogren's syndrome.
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Oxypyrronium bromide
L.D. 3055,Immetropan,LD 3055,LD3055,LD-3055
T25912561-43-3
Oxypyrronium bromide is an anticholinergic and spasmolytic agent containing quaternary ammonium. In animal models it inhibited gastric motility, hypotension induced by vagus stimulation or intravenation of acetylcholine; salivation induced by chorda tympani nerve stimulation, and contraction elicited by preganglionic cervical sympathetic nerve stimulation.
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6-8 weeks
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Methylatropine (nitrate)
T3620452-88-0
Methylatropine is an antagonist of muscarinic acetylcholine receptors (IC50= <0.1 nM in a radioligand binding assay using isolated porcine brain membranes) and a derivative of atropine .1,2It reduces acetylcholine-induced decreases in blood pressure in rats when administered intravenously with an ED50value of 5.5 μg/kg.2Methylatropine reduces salivation, induces mydriasis, and increases heart rate in dogs.3 1.Schmeller, T., Sporer, F., Sauerwein, M., et al.Binding of tropane alkaloids to nicotinic and muscarinic acetylcholine receptorsPharmazie50(7)493-495(1995) 2.Brezenoff, H.E., Xiao, Y.-F., and Vargas, H.A comparison of the central and peripheral antimuscarinic effects of atropine and methylatropine injected systemically and into the cerebral ventriclesLife Sci.42(8)905-911(1988) 3.Albanus, L.Central and peripheral effects of anticholinergic compoundsActa Pharmacol. Toxicol. (Copenh)28(4)305-326(1970)
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ASP9133
T715411047677-07-5
ASP9133 is a long-acting muscarinic antagonist (LAMA) which shows more selective inhibition of bronchoconstriction against salivation and more rapid onset of action than tiotropium bromide.
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6-8 weeks
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Glycopyrrolate-d5
Glycopyrronium Bromide-d5
TMIH-0256
Glycopyrrolate-d5 is a deuterated compound of Glycopyrrolate. Glycopyrrolate has a CAS number of 596-51-0. Glycopyrrolate is a muscarinic antagonist used as an antispasmodic, in some disorders of the gastrointestinal tract, and to reduce salivation with some anesthetics.
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7-10 days
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Anisodamine hydrochloride
6-Hydroxyhyoscyamine hydrochloride
TN7625131674-05-0
Anisodamine hydrochloride, an anticholinergic and α1 adrenergic receptor antagonist, is used for enhancing blood flow in circulatory disorders like septic shock. It exhibits a range of pharmacological effects similar to Atropine and Scopolamine, including the inhibition of salivation, gastrointestinal and sweat secretion, gastrointestinal motility, respiratory secretion, and urinary bladder contraction in vivo [1].
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