T79684 |
5-HT6R antagonist 1
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98%
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Compound 8 (5-HT6R antagonist 1), a 5-HT6R antagonist (K i : 5 nM), not only demonstrates inhibition of platelet aggregation and excellent metabolic stability bu...
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T79802 |
5-HT2C agonist-3
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2104810-18-4
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98%
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5-HT2C agonist-3 ((+)-19), a selective 5-HT2C agonist (EC 50: 24 nM, Ki: 78 nM), exhibits antipsychotic-like activity by blocking amphetamine-induced hyperactivi...
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T79803 |
5-HT2C agonist-3 free base
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2104810-17-3
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98%
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5-HT2C agonist-3 ((+)-19) free base, a selective 5-HT2C agonist (EC50: 24 nM, Ki: 78 nM), exhibits antipsychotic drug-like activity and inhibits Amphetamine-indu...
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T79804 |
5-HT2 agonist-1
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2708279-78-9
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98%
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Compound 24, a 5-HT2 agonist-1, selectively activates 5-HT2A, 5-HT2B, and 5-HT2C receptors with IC50 values of 10 nM, 8.3 nM, and 1.6 nM, respectively. The free ...
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T79805 |
5-HT2 agonist-1 free base
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2708279-77-8
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98%
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Compound 24 (5-HT2 agonist-1 free base) is a potent agonist for 5-HT2A, 5-HT2B, and 5-HT2C receptors, exhibiting IC50 values of 10 nM, 8.3 nM, and 1.6 nM, respec...
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T79806 |
5-HT2A&5-HT2C agonist-1
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1640-02-4
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98%
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5-HT2A&5-HT2C agonist-1 (Example 2) is a dual-acting agent targeting the 5-HT2A and 5-HT2C receptors with respective IC50 values of 196 nM and 0.9 nM. It is appl...
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T79838 |
(S)-Bexicaserin
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2035818-21-2
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98%
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(S)-Bexcaserin (compound 2) serves as a 5-HT2C receptor agonist, presenting research possibilities in obesity and psychiatric disorders [1].
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T15026 |
Cyamemazine
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3546-03-0
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98%
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Cyamemazine, contains the phenothiazine chromophore, is a neuroleptic agent used as an anxiolytic. Cyamemazine is a potent 5-HT3 (Ki: 12 nM), 5-HT2A (Ki: 1.5 nM)...
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T81335 |
PZ-1922
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98%
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PZ-1922 (Compound 16), able to cross the blood-brain barrier, is a dual antagonist for 5-HT6R and 5-HT3R with K i values of 17 nM and 0.45 nM, respectively. It a...
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T12262L |
NPS ALX Compound 4a dihydrochloride
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1781934-44-8
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98%
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NPS ALX Compound 4a dihydrochloride is a potent and selective antagonist of 5-HT6 receptor (IC50 of 7.2 nM)
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T10114 |
3-Hydroxy agomelatine
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166526-99-4
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98%
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3-Hydroxy agomelatine is an Agomelatine metabolite and a 5-HT2C receptor antagonist (IC50: 3.2 μM; Ki: 1.8 μM).
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TN3393 |
Alpha-Yohimbine
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131-03-3
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98%
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Alpha-Yohimbine is a 5-HT1A receptor agonist, it is strong selective 2-adrenoceptor antagonist. Alpha-Yohimbine possess aphrodisiac effect.
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T12716 |
RG-12915
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136174-04-4
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98%
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RG-12915 is a selective antagonist of 5-HT3(IC50 value of 0.16 nM).
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T12859 |
SB 243213 hydrochloride
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200940-23-4
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98%
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SB 243213 hydrochloride is an orally active, selective and high-affinity antagonist of 5-hydroxytryptamine (5-HT)2C receptor(pKi of 9.37 and a pKb of 9.8).It has...
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T11216 |
Eplivanserin (mixture)
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130581-13-4
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98%
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Eplivanserin mixture is a selective serotonin reuptake inhibitor and a 5-HT2A receptor antagonist,
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T16683 |
Pumosetrag Hydrochloride
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194093-42-0
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98%
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Pumosetrag Hydrochloride is an orally available 5-HT3 partial agonist. It is developed for the treatment of irritable bowel syndrome and gastroesophageal reflux ...
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T12046 |
Mirtazapine D3
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1216678-68-0
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98%
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Mirtazapine D3 is a deuterium labeled Mirtazapine. Mirtazapine is an inhibitor of 5-HT receptor .
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T10612 |
Brexpiprazole S-oxide
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1191900-51-2
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98%
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Brexpiprazole S-oxide (DM-3411) is a main metabolite of Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Kis: 0.12 nM an...
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T6959 |
PRX-08066 Maleic acid
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866206-55-5
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98%
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|
PRX-08066 Maleic acid is a selective 5-HT2B receptor antagonist with IC50 of 3.4 nM, prevents the severity of pulmonary arterial hypertension in the MCT rat mode...
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T12806 |
(S)-Mirtazapine D3
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T12806
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98%
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(S)-Mirtazapine D3 is a deuterium labeled (S)-Mirtazapine. (S)-Mirtazapine is a stereoselective antagonist of 5-HT2 receptor. (S)-Mirtazapine is metabolized by C...
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