Ketanserin tartrate

Serotonin 5HT2A Antagonist

Catalog No. SIH-618

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CAS No. 83846-83-7
Molecular Formula C22H22FN3O3 • C4H6O6
SKU: SIH-618 Categories: ,

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SIH-618-Ketanserin-tartrate-Chemical-Structure
Product Name Ketanserin tartrate
Description

Serotonin 5HT2A Antagonist

Purity >98% (HPLC); NMR (conforms)
CAS No. 83846-83-7
Molecular Formula C22H22FN3O3 • C4H6O6
Molecular Weight 545.5
Field of Use Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.

Properties

Storage Temperature -20ºC
Shipping Temperature Shipped Ambient
Product Type Antagonist
Solubility May be dissolved in DMSO (30 mg/ml); or Water (5 mg/ml)
Source Synthetic
Appearance White powder
SMILES C1CN(CCC1C(=O)C2=CC=C(C=C2)F)CCN3C(=O)C4=CC=CC=C4NC3=O.C(C(C(=O)O)O)(C(=O)O)O
InChI InChI=1S/C22H22FN3O3.C4H6O6/c23-17-7-5-15(6-8-17)20(27)16-9-11-25(12-10-16)13-14-26-21(28)18-3-1-2-4-19(18)24-22(26)29;5-1(3(7)8)2(6)4(9)10/h1-8,16H,9-14H2,(H,24,29);1-2,5-6H,(H,7,8)(H,9,10)
InChIKey KMTLTEVOQLMYRS-UHFFFAOYSA-N
Safety Phrases Classification: Danger.

Hazard Statements: H301
Precautionary Statements: P264 - P270 - P301 + P310 - P405 - P501
Cite This Product Ketanserin tartrate (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-618)

Biological Description

Alternative Names 3-[2-[4-(4-Fluorobenzoyl)-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione, tartrate; R41468
Research Areas Ion Channels, Neuroscience, Neurotransmission, Neurotransmitter Receptors, Potassium Channels
PubChem ID 135348
Scientific Background Ketanserin tartrate is a selective antagonist of the serotonin 5-HT2A receptor, with additional affinity for the 5-HT1Dα receptor. While primarily studied for its cardiovascular effects, including treatment of hypertension post-coronary artery surgery, Ketanserin has gained attention in neuroscience for its ability to modulate serotonergic signaling. It has been used to investigate the cognitive and perceptual effects of 5-HT2A receptor activation, including disruption of hallucinogenic responses. Its role in modulating serotonin pathways makes it a valuable tool in neuropsychiatric and neuropharmacological research.
References 1. Leysen JE., et al. (1981) Life Sci. 28:1015.
2. Zgombick JM., et al. (1995) Eur. J. Pharmacol. 291:9.
3. Vandenbroucke G., et al.(1994) J. Cardiothorac. Vasc. Anesth. 8: P324.
4. Quednow BB.,et al. (2012) Neuropsychopharmacology. 37:630.

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