Details
Stereochemistry | ACHIRAL |
Molecular Formula | C29H27F2N3O |
Molecular Weight | 471.541 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(CCN2CCC(CC2)=C(C3=CC=C(F)C=C3)C4=CC=C(F)C=C4)C(=O)N5C=CC=CC5=N1
InChI
InChIKey=ZGUPMFYFHHSNFK-UHFFFAOYSA-N
InChI=1S/C29H27F2N3O/c1-20-26(29(35)34-16-3-2-4-27(34)32-20)15-19-33-17-13-23(14-18-33)28(21-5-9-24(30)10-6-21)22-7-11-25(31)12-8-22/h2-12,16H,13-15,17-19H2,1H3
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/8853256
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8853256
Seganserin was developed as a specific serotonin 5HT2 receptor antagonist. It was tested neuropharmacologically in thioacetamide-induced acute liver failure in rats. Obtained results have shown that seganserin had no effect in encephalopathic rats.
Approval Year
PubMed
Title | Date | PubMed |
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Characterization of flufylline, fluprofylline, ritanserin, butanserin and R 56413 with respect to in-vivo alpha 1-,alpha 2- and 5-HT2-receptor antagonism and in-vitro affinity for alpha 1-,alpha 2- and 5-HT2-receptors: comparison with ketanserin. | 1986 May |
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Effects of seganserin, a 5-HT2 antagonist, and temazepam on human sleep stages and EEG power spectra. | 1989 Nov 21 |
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Modulation of hepatic encephalopathy in rats with thioacetamide-induced acute liver failure by serotonin antagonists. | 1996 Jul |
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Effect of 5-HT1A and 5-HT2A/2C receptor modulation on neuroleptic-induced vacuous chewing movements. | 2001 Sep 28 |
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C66885
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C046301
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ACTIVE MOIETY