44 Results for "

5-HT derivative

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "5-HT derivative" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-B0068
CAS No.: 123040-16-4
Synonyms: Y-25130 hydrochloride
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Azasetron (Y-25130) hydrochloride, a benzamide derivative, is a potent and selective 5-HT3 receptor antagonist. Azasetron is used in the study for Chemotherapy-induced nausea and vomiting (CINV) .
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1
1 Cited Publications
Cat. No.: HY-B0781
CAS No.: 58-33-3
Promethazine hydrochloride is an orally active phenothiazine derivative with antihistaminic (H1), sedative, antiemetic, anticholinergic, and antimotion sickness properties. Promethazine hydrochloride is a potent H1 receptor antagonist and a mAChR antagonist. It also has a certain affinity for 5-HT2A and 5-HT2C receptors .
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1
1 Cited Publications
Cat. No.: HY-156562A
CAS No.: 2906227-87-8
Purity:  99.91%
Synonyms: 5-Propargyltryptamide formic
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology

5-PT (5-Propargyltryptamide) formic is an alkyne-functionalized 5-HT (HY-B1473A) derivative and serotonylation substrate, taken up by living cells. 5-PT formic conjugated to a biotin enables identification of serotonylated proteins via copper-click chemistry and mass spectrometry. 5-PT formic labels and isolates serotonylated cells in alveolar epithelial cells for proteomic analysis. 5-PT formic can be used for the research of bronchopulmonary dysplasia .
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1
1 Cited Publications
Cat. No.: HY-19469
CAS No.: 359625-79-9
Synonyms: CYR-101; MIN-101; MT-210
Research Areas:  

Neurological Disease

Roluperidone (CYR-101) is a novel cyclic amide derivative that has high equipotent affinities for 5-HT2A and sigma-2 receptors (Ki of 7.53 nM and 8.19 nM for 5-HT2A and sigma-2, respectively).
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Cat. No.: HY-W018864
CAS No.: 51364-51-3
Research Areas:  

Others

Tris(dibenzylideneacetonyl)bis-palladium is a catalyst that catalyzes the coupling reaction of N-methyl-2-pyrrolidinone (NMP). Tris(dibenzylideneacetonyl)bis-palladium participates in the synthesis of camptothecin derivatives, 5-HT antagonists, etc .
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Cat. No.: HY-100703
CAS No.: 1893-33-0
Purity:  99.89%
Synonyms: Floropipamide; McN-JR 3345; R 3345
Research Areas:  

Neurological Disease

Pipamperone (Floropipamide) is a butyrophenone derivative and high-affinity antagonist of 5-HT2A receptor (pKi=8.2) and D4 receptor (pKi=8.0). Pipamperone is also a low-affinity antagonist of D2 receptor (pKi=6.7). Pipamperone affects neurotransmitter functions and exerts antipsychotic activity. Pipamperone is used in the research of mental disorders such as autism-related behavioral disorders and Alzheimer's disease .
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Cat. No.: HY-156562
CAS No.: 92085-05-7
Synonyms: 5-Propargyltryptamide
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology

5-PT (5-Propargyltryptamide) is an alkyne-functionalized 5-HT (HY-B1473A) derivative and serotonylation substrate, taken up by living cells. 5-PT conjugated to a biotin enables identification of serotonylated proteins via copper-click chemistry and mass spectrometry. 5-PT labels and isolates serotonylated cells in alveolar epithelial cells for proteomic analysis. 5-PT can be used for the research of bronchopulmonary dysplasia .
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Cat. No.: HY-136621
CAS No.: 3880-76-0
Purity:  99.69%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

5-HT1A modulator 2 hydrochloride, a derivative of 8-OH-DPAT (HY-112061), is a modulator of 5-HT1A with a Ki of 53 nM for 5-HT1A binding .
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Cat. No.: HY-111419
CAS No.: 1176326-76-3
Purity:  99.72%
Research Areas:  

Neurological Disease

DSP-1053, a benzylpiperidine derivative, is a potent Serotonin Transporter (SERT) inhibitor with a Ki of 1.02 nM. DSP-1053 shows partial 5-HT1A receptor agonistic activity with a Ki of 5.05 nM. DSP-1053 has antidepressant activity .
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Cat. No.: HY-123207
CAS No.: 82900-57-0
Target:  

5-HT Receptor

Research Areas:  

Metabolic Disease

BP 554 is a selective 5-HT1A receptor agonist and Piperazine derivative. BP 554 leads to hypothermia .
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Cat. No.: HY-103118
CAS No.: 313984-77-9
Purity:  98.92%
Target:  

5-HT Receptor Apoptosis

Research Areas:  

Neurological Disease Cancer

PU02, a derivative of 6-MP (HY-13677), is a negative allosteric modulator (NAM) of 5-HT3 receptor, with IC50 values of 0.36 and 0.73 μM in HEK293 cells transfected with human 5-HT3A and 5-HT3AB receptors respectively .
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Cat. No.: HY-106136
CAS No.: 118702-11-7
Synonyms: PD-6735; LY-156735
Research Areas:  

Neurological Disease

TIK-301 (PD-6735) is a chlorinated melatonin derivative and a potent, high-affinity and orally active melatonin MT1 and MT2 receptors agonist with Kis of 0.081 nM and 0.042 nM, respectively. TIK-301 is also a 5-HT2B/5-HT2C receptors antagonist with antidepressant action. TIK-301 has the potential for sleep disorders and other circadian rhythm disorders treatment .
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Cat. No.: HY-165624
CAS No.: 140221-50-7
Research Areas:  

Neurological Disease

LY-41 is a 2-aminotetralin (HY-W022362) derivative related to 8-OH-DPAT (HY-112061). LY-41 decreases 5-HT synthesis. LY-41 induces 5-HT motor syndrome. (R)-LY-41 and (S)-LY-41 are novel 5-HT1A receptor agonists .
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Cat. No.: HY-137162
CAS No.: 84625-59-2
Dotarizine is a novel Piperazine (HY-B0912) derivative and antimigraine agent. Dotarizine exhibits Ca 2+ channel blocking properties. Dotarizine decreases the release of lactate dehydrogenase. Dotarizine shows 5-HT receptor blocking effect .
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Cat. No.: HY-165624A
CAS No.: 136296-40-7
(S)-LY-41, R-enantiomer of LY-41 (HY-165624), is 2-Sminotetralin (HY-W022362) derivative and 8-OH-DPAT (HY-112061) analogue. (S)-LY-41 is a potent and selective 5-HT1A receptor agonist. (S)-LY-41 can reduce the accumulation of 5-hydroxytryptophan (the precursor for 5-HT synthesis) in the rat brain induced by decarboxylase inhibitors (NSD 1015). (S)-LY-41 can lower the body temperature of rats and inhibit the escape response from the cage. (S)-LY-41 can induce the 5-HT behavioral syndrome. (S)-LY-41can be used for the research of neurological disease, such as depression and anxiety .
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Cat. No.: HY-165624B
CAS No.: 136296-43-0
(R)-LY-41, R-enantiomer of LY-41 (HY-165624), is 2-Sminotetralin (HY-W022362) derivative and 8-OH-DPAT (HY-112061) analogue. (R)-LY-41 is a potent and selective 5-HT1A receptor agonist. (R)-LY-41 can reduce the accumulation of 5-hydroxytryptophan (the precursor for 5-HT synthesis) in the rat brain induced by decarboxylase inhibitors (NSD 1015). (R)-LY-41 can lower the body temperature of rats and inhibit the escape response from the cage. (R)-LY-41 can induce the 5-HT behavioral syndrome but is weaker than (S)-LY-41 (HY-165624A). (R)-LY-41 can be used for the research of neurological disease, such as depression and anxiety .
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Cat. No.: HY-W284026
CAS No.: 130445-55-5
PIM-35 is a derivative of Indole (HY-W001132). PIM-35 significantly inhibits serotonin (5HT) and dopamine (DA) uptake with a weak inhibitory effect on noradrenaline (NA) uptake.PIM-35 has antidepressant activity and can be used for depression research .
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Cat. No.: HY-W128798
CAS No.: 127-77-5
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Sulfabenz (Compound 9) is an amine-substituted N1-phenylsulfonyl indole derivative. Sulfabenz has binding activity to human 5-HT6 serotonin receptor (Ki: 200 nM). Sulfabenz can be used to study the ligand binding mechanism of 5-HT6 receptor and 5-HT6 receptor-related neurological diseases .
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Cat. No.: HY-169785
CAS No.: 65882-39-5
Synonyms: 7-TMT
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

7-Methyl DMT (7-TMT) is a 5-HT2 receptor agonist. Structurally, 7-Methyl DMT is a tryptamine derivative. It can be used as an analytical reference standard for the psychoactive substance DOM. 7-Methyl DMT is also used in research in the field of neurological diseases .
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Cat. No.: HY-34763
CAS No.: 70500-72-0
Synonyms: 7-Hydroxyquinolinone; 2,7-Dihydroxyquinoline
Target:  

Drug Derivative

Research Areas:  

Others

7-Hydroxycarbostyril (7-Hydroxy-2(1H)-quinolinone) (Compound 7) is a quinolinone derivative. 7-Hydroxycarbostyril can be used for synthesis of Brexpiprazole (HY-15780). Brexpiprazole, a typical orally active antipsychotic agent, is a partial agonist of human 5-HT1A and dopamine D2L receptor .
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