100 Results for "

5-HT7 Receptor

" in MedChemExpress (MCE) Product Catalog:
Products (100)

100 Results for "5-HT7 Receptor" in MCE Product Catalog:

Cat. No.: HY-B0032AS
CAS No.: 1132654-54-6
Synonyms: SM-13496-d8
Lurasidone-d8 is deuterium labeled Lurasidone. Lurasidone (SM-13496) is an antagonist of both dopamine D2 and 5-HT7 with IC50s of 1.68 and 0.495 nM, respectively. Lurasidone (SM-13496) is also a partial agonist of 5-HT1A receptor with an IC50 of 6.75 nM.
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Cat. No.: HY-15414AS
Synonyms: Lu AA21004-d8 hydrobromide
Vortioxetine-d8 (Lu AA 21004-d8) hydrobromide is the deuterated form of Vortioxetine. Vortioxetine (Lu AA 21004) is an antagonist of 5-HT3A and 5-HT7 receptors (Ki: 3.7 nM, 19 nM) and an inhibitor of 5-hydroxytryptamine transporter (SERT) (Ki: 1.6 nM), as well as a 5-HT1A agonist and a partial 5-HT1B agonist (Ki: 15 nM, 33 nM) .
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Cat. No.: HY-W052508R
CAS No.: 5747-48-8
Synonyms: N-Desalkylquetiapine (Standard)
Research Areas:  

Neurological Disease

Norquetiapine is an antidepressant and neuroprotective agent and is the active metabolic component of Quetiapine (HY-14544). Norquetiapine is also a partial 5-HT1A receptor agonist, and a presynaptic α2, 5-HT2C and 5-HT7 b> Receptor antagonist. Norquetiapine can also selectively inhibit norepinephrine transporter (NET), inhibit norepinephrine reuptake, and has potential inhibitory effects on bipolar depression, major depressive disorder, and generalized anxiety disorder. Norquetiapine demonstrated in vivo activity in forced swimming in mice and learned helplessness tests in rats .
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Cat. No.: HY-117046
CAS No.: 1025725-91-0
AVN-101 is a potent, brain-penetrant and orally active 5-HT7 receptor antagonist (Ki of 153 pM), with slightly lesser potency toward 5-HT6, 5-HT2A, and 5HT-2C receptors (Ki values of 2.04 nM, 1.56  nM, and 1.17  nM, respectively). AVN-101 also exhibits a rather high affinity toward histamine H1 (Ki of 0.58 nM) and adrenergic α2A, α2B, and α2C (Ki= 0.41-3.6 nM) receptors. AVN-101 can be studied in such diseases as general anxiety disorders, depression, schizophrenia, Alzheimer’s disease, and multiple sclerosis .
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Cat. No.: HY-101009
CAS No.: 19728-88-2
Synonyms: Metitepine maleate; Ro-8-6837 maleate
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Methiothepin maleate is a potent and non-selective 5-HT2 receptor antagonist, with pKds of 7.10 (5-HT1A), 7.28 (5HT1B), 7.56 (5HT1C), 6.99 (5HT1D), 7.0 (5-HT5A), 7.8 (5-HT5B), 8.74 (5-HT6), and 8.99 (5-HT7), and pKis of 8.50 (5HT2A), 8.68 (5HT2B), and 8.35 (5HT2C).
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Cat. No.: HY-111491
CAS No.: 20229-30-5
Synonyms: Metitepine; Ro 8-6837
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Methiothepin (Metitepine; Ro 8-6837) is a potent and non-selective 5-HT2 receptor antagonist, with pKds of 7.10 (5-HT1A), 7.28 (5HT1B), 7.56 (5HT1C), 6.99 (5HT1D), 7.0 (5-HT5A), 7.8 (5-HT5B), 8.74 (5-HT6), and 8.99 (5-HT7), and pKis of 8.50 (5HT2A), 8.68 (5HT2B), and 8.35 (5HT2C).
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Cat. No.: HY-B1658B
CAS No.: 158930-09-7
Synonyms: (R)-Frovatriptan succinate; SB 209509 succinate; VML 251 succinate
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Frovatriptan succinate ((R)-Frovatriptan succinate) is a potent, high affinity, selective and orally active 5-HT1B (pK50 of 8.2) and 5-HT1D receptor agonist. Frovatriptan succinate exhibits >10-fold selectivity for 5-HT1B and 5-HT1D over 5-HT1A, 5-HT1F, and 5-HT7 and >1000-fold selectivity over other 5-HT, dopamine, histamine H1, and α1-adrenoceptor. Frovatriptan succinate has the potential for migraine research .
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Cat. No.: HY-172339
Synonyms: 4-Acetoxy DALT hydrochloride
4-AcO-DALT hydrochloride is a tryptamine compound with psychoactive effects. 4-AcO-DALT hydrochloride inhibits 5-HT receptors, alpha receptors, dopamine receptors, histamine receptor 1 (H1), muscarinic M2 receptor and Sigma 2 receptor. 4-AcO-DALT hydrochloride shows Ki values of 582 nM, 2689 nM, 2099 nM, 2116 nM, 958 nM, 137 nM, 824 nM, 479 nM, 406 nM, 874 nM, 4190 nM, 482 nM, 214 nM, 803 nM, 4522 nM, 1907 nM for 5-HT1B, 5-HT1D, 5-HT1E, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT6, 5-HT7A, H1, Sigma 2, α2A, α2B, α2C, D2, D3 receptors .
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Cat. No.: HY-147399
CAS No.: 1206846-61-8
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

5-HT7 agonist 2 is a potent 5-HT7 receptor agonist with an IC50 value of 28.7 nM. 5-HT7 agonist 2 can be used for research of central nervous system (CNS) disorders .
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Cat. No.: HY-103119
CAS No.: 1386928-34-2
Target:  

5-HT Receptor

Research Areas:  

Others

LP-20 hydrochloride acts as a ligand for the 5-HT7 receptor.
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Cat. No.: HY-19889A
CAS No.: 851373-91-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

JNJ-18038683 free base is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with pKis of 8.19, 8.20 for rat and human 5-HT7 in HEK293 cells, respectively.
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Cat. No.: HY-136678
CAS No.: 201038-58-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

SB 258741 is an efficient and highly selective 5-HT7 receptor (pKi = 8.5) antagonist.
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Cat. No.: HY-103105A
Purity:  ≥99.0%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LP 12 hydrochloride hydrate is a potent and selective 5-HT7 receptor agonist with a Ki of 0.13 nM. LP 12 hydrochloride hydrate displays selectivity for 5-HT7 over D2, 5-HT1A and 5-HT2A receptors (Ki values are 224 nM, 60.9 nM and >1000 nM, respectively) .
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Cat. No.: HY-103105
CAS No.: 1185136-22-4
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LP 12 hydrochloride (compound 21) is a potent and selective 5-HT7 receptor agonist with a Ki of 0.13 nM. LP 12 hydrochloride displays selectivity for 5-HT7 over D2, 5-HT1A and 5-HT2A receptors (Ki values are 224 nM, 60.9 nM and >1000 nM, respectively) .
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Cat. No.: HY-103148
CAS No.: 137328-52-0
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LY215840, a 5-HT7 receptor ligand and a 5-HT2 receptor antagonist, blocks serotonin-induced relaxation in canine coronary artery .
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Cat. No.: HY-116581
CAS No.: 1386927-90-7
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

5-HT7R antagonist 4 (Compound 4) is a potent 5-HT7 receptor antagonist (Ki=2.6 nM) with low binding affinity for the 5-HT1A receptor (Ki= 476 nM). 5-HT7R antagonist 4 is promising for research of neurological diseases .
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Cat. No.: HY-14545B
CAS No.: 2974362-88-2
Research Areas:  

Neurological Disease

SEP4199 is an orally active 5-HT7 receptor ligand, with a Ki value of 66 nM for human 5-HT7R and 16 nM for human D2R. SEP4199 mediates antidepressant effects. SEP4199 is applicable for the research of bipolar depression .
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Cat. No.: HY-124135
CAS No.: 446020-51-5
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

SB-656104 is a potent antagonist of 5-HT7 receptor, with the pKi of 8.70, blocking 5-carboxamidotryptamine (5-CT) stimulated adenylyl cyclase activity .
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Cat. No.: HY-G0002S
CAS No.: 2070009-33-3
Lurasidone metabolite 14326-d8 is a deuterium-labeled form of Lurasidone metabolite 14326 (HY-G0002). Lurasidone metabolite 14326 is a minor active metabolite of Lurasidone (HY-B0032A) generated via metabolism by CYP3A4. Lurasidone metabolite 14326 shares similar receptor-binding properties with Lurasidone, acting as an antagonist of the dopamine D2 receptor (dopamine D2 receptor), an antagonist of the serotonin 5-HT2A and 5-HT7 receptors (5-HT2A and 5-HT7 receptor), and a partial agonist of the serotonin 5-HT1A receptor. Lurasidone metabolite 14326 can be used in the research of schizophrenia and bipolar depression .
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Cat. No.: HY-109167A
CAS No.: 2129505-46-8
Synonyms: (R)-Amisulpride hydrochloride; (R)-Esamisulpride hydrochloride; (R)-DAN 2163 hydrochloride
Research Areas:  

Neurological Disease

Aramisulpride hydrochloride is a 5-HT7 receptor antagonist with a Ki value of 22 nM. Aramisulpride hydrochloride is a D2/D3 receptor antagonist with a Ki value of 140 nM for D2R and a Ki value of 13.9 nM for D3R. Aramisulpride hydrochloride can be used in psychiatric research .
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