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varenicline

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
  • Cell Research
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    TargetMol | Inhibitors_Agonists
Varenicline
CP 526555, CP526555
T4246L249296-44-4
Varenicline (CP 526555) is a selective partial agonist of the α4β2 nAChR and a full agonist of the α3β4 nAChR and α7 nAChR to help smokers with cardiovascular disease and COPD quit smoking.
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1-2 weeks
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Varenicline Tartrate
Champix tartrate, Chantix tartrate, CP 526555-18
T1657375815-87-5
Varenicline Tartrate (CP 526555-18) is a benzazepine derivative that functions as an ALPHA4 BETA2 NICOTINIC RECEPTOR partial agonist. It is used for SMOKING CESSATION.
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Varenicline Hydrochloride
T23502230615-23-3
Varenicline Hydrochloride is a partial agonist of α4β2 nicotinic receptor.
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7-10 days
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Varenicline dihydrochloride
T4246866823-63-4
Varenicline dihydrochloride is a Selective α4β2 nicotinic acetylcholine receptor partial agonist.
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Hydroxy Varenicline
2-Hydroxyvarenicline
T85294357424-21-6
Hydroxy varenicline, a metabolite of the nicotinic acetylcholine receptor (nAChR) agonist varenicline, functions within the biochemical pathway by interacting with nAChR sites.
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8-10 weeks
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Varenicline crbamoyl β-D-glucuronide
TSW-00734535920-98-0
Varenicline crbamoyl β-D-glucuronide is a biochemical reagent used in glycoscience research. Glycoscience explores the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.
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7-10 days
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uPSEM 792 hydrochloride
T36810
Ultrapotent PSEM (uPSEM) agonist for PSAM4-GlyR and PSAM4-5HT3 (Ki = 0.7 nM for PSAM4-GlyR and <10 nM for PSAM4-5HT3). Exhibits >10,000-fold agonist selectivity for PSAM4-GlyR over α7-GlyR, α7-5HT3, and 5HT3-R, and 230-fold selectivity over α4β2 nAChR. Also weak partial agonist (~10 %) at α4β2 nAChR. Retains the potency of varenicline (Cat.No. 3754) for PSAM4-GlyR with enhanced chemogenetic selectivity. Does not act as a substrate for P-glycoprotein pumps. Silences neurons in vivo. Brain-penetrant. Magnus et al (2019) Ultrapotent chemogenetics for research and potential clinical applications. Science doi: 10.1126/science PMID:30872534
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