200 Results for "

depressor

" in MedChemExpress (MCE) Product Catalog:
Products (200)

200 Results for "depressor" in MCE Product Catalog:

19
19 Publications Verification
Cat. No.: HY-16900
CAS No.: 61413-54-5
Synonyms: (R,S)-Rolipram; (±)-Rolipram; ZK 62711
Rolipram is a PDE4 inhibitor, with blood-brain barrier permeability, that reverses β-amyloid-induced learning and memory impairment in rats. Rolipram elevates intracellular cAMP and clevels and regulates the cAMP/CREB signaling pathway, thereby alleviating neuroinflammation and apoptotic responses. Rolipram promotes neuronal differentiation of human bone marrow mesenchymal stem cells and inhibits Methamphetamine- and morphine-induced hyperlocomotion in mice. Rolipram also reduces the viability of glioblastoma stem-like cells and enhances Bevacizumab (HY-P9906)-induced cell death. Rolipram inhibits the expression of proinflammatory cytokines and enhances central noradrenergic transmission. Rolipram is mainly used in studies related to various central nervous system diseases including Alzheimer's disease, major depressive disorder, glioblastoma multiforme, and multiple sclerosis .
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18
18 Cited Publications
Cat. No.: HY-B0176A
CAS No.: 79559-97-0
Target:  

Serotonin Transporter

Research Areas:  

Neurological Disease Cancer

Sertraline hydrochloride is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. Sertraline hydrochloride is researched for a number of diseases, such as major depressive disorder and obsessive .
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12
12 Cited Publications
Cat. No.: HY-B0161A
CAS No.: 136434-34-9
Synonyms: (S)-Duloxetine hydrochloride; LY-248686 hydrochloride
Target:  

Serotonin Transporter

Research Areas:  

Neurological Disease Cancer

Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a serotonin-norepinephrine reuptake inhibitor (SNRI) with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD) .
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12
12 Cited Publications
Cat. No.: HY-B0161
CAS No.: 116539-59-4
Synonyms: LY248686
Target:  

Serotonin Transporter

Research Areas:  

Neurological Disease Cancer

Duloxetine is a serotonin-norepinephrine reuptake inhibitor with a Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD) .
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10
10 Cited Publications
Cat. No.: HY-B0591
CAS No.: 19982-08-2
Target:  

iGluR

Research Areas:  

Neurological Disease

Memantine is an orally active, noncompetitive N-methyl-D-aspartate receptor (NMDAR) antagonist. Memantine can be used for the research of moderate-to-severe Alzheimer's disease (AD) .
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10
10 Cited Publications
Cat. No.: HY-14199
CAS No.: 14611-52-0
Purity:  99.94%
Synonyms: Deprenyl hydrochloride; (-)-Selegiline hydrochloride; (-)-Deprenyl hydrochloride
Target:  

Monoamine Oxidase

Research Areas:  

Neurological Disease

Selegiline (Deprenyl) hydrochloride is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. Selegiline hydrochloride exhibits 450-flod selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline hydrochloride can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder .
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9
9 Cited Publications
Cat. No.: HY-17038
CAS No.: 138112-76-2
Synonyms: S-20098
Agomelatine (S-20098) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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9
9 Cited Publications
Cat. No.: HY-17038A
CAS No.: 1176316-99-6
Synonyms: S-20098 hydrochloride
Agomelatine hydrochloride (S-20098 hydrochloride) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine hydrochloride is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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9
9 Cited Publications
Cat. No.: HY-17038B
CAS No.: 824393-18-2
Synonyms: S-20098 L(+)-Tartaric acid
Agomelatine L(+)-Tartaric acid (S-20098 L(+)-Tartaric acid) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively . Agomelatine L(+)-Tartaric acid is a selective 5-HT2C receptor antagonist with pKis of 6.4 and 6.2 at native (porcine) and cloned, human 5-HT2C receptors, respectively .
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6
6 Cited Publications
Cat. No.: HY-14262
CAS No.: 163521-12-8
Purity:  99.84%
Synonyms: EMD 68843; SB659746A
Research Areas:  

Neurological Disease

Vilazodone (EMD 68843; SB 659746A) is a potent, selective and orally active serotonin reuptake inhibitor (SSRI) and partial 5-HT1A receptor agonist. Vilazodone exhibits antidepressant efficacy in vivo can be used for the research of major depressive disorder (MDD) and affective disorders .
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6
6 Cited Publications
Cat. No.: HY-B0478A
CAS No.: 19794-93-5
Synonyms: AF-1161 free base
Trazodone (AF-1161 free base) is a triazolopyridine derivative that belongs to the class of serotonin receptor antagonists and reuptake inhibitors (SARIs). Trazodone has anti-depressant and anti-insomnious activity. Trazodone exerts antagonistic properties against a1- and a2-adrenergic receptors and histamine H1 receptors, with minimal anticholinergic effects .
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3
3 Cited Publications
Cat. No.: HY-N0139
CAS No.: 7085-55-4
Synonyms: Trihydroxyethylrutin
Troxerutin, also known as vitamin P4, is a tri-hydroxyethylated derivative of natural bioflavonoid rutins which can inhibit the production of reactive oxygen species (ROS) and depress ER stress-mediated NOD activation.
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3
3 Cited Publications
Cat. No.: HY-N0740
CAS No.: 6681-15-8
Jatrorrhizine chloride is an alkaloid isolated from Coptis chinensis with neuroprotective, antimicrobial, antiplasmodial and antioxidant activities . Jatrorrhizine chloride is a potent and orally active inhibitor of AChE (IC50=872 nM) over >115-fold selectivity for BuChE . Jatrorrhizine chloride reduces uptake of serotonin (5-HT) and norepinephrine (NE) via inhibition of uptake-2 transporters .
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3
3 Cited Publications
Cat. No.: HY-N0749A
CAS No.: 483-43-2
Jatrorrhizine hydroxide is an alkaloid isolated from Coptis chinensis with neuroprotective, antimicrobial, antiplasmodial and antioxidant activities . Jatrorrhizine hydroxide is a potent and orally active inhibitor of AChE (IC50=872 nM) over >115-fold selectivity for BuChE . Jatrorrhizine hydroxide reduces uptake of serotonin (5-HT) and norepinephrine (NE) via inhibition of uptake-2 transporters .
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2
2 Cited Publications
Cat. No.: HY-15856B
CAS No.: 2413-38-9
Purity:  98.52%
Synonyms: Flupenthixol dihydrochloride
Research Areas:  

Neurological Disease Cancer

Flupentixol is an orally active D1/D2 dopamine receptor antagonist and new PI3K inhibitor (PI3Kα IC50=127 nM). Flupentixol shows anti-proliferative activity to cancer cells and induces apoptosis. Flupentixol can also be used in schizophrenia, anxiolytic and depressive research .
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2
2 Cited Publications
Cat. No.: HY-109046
CAS No.: 1038984-31-4
Purity:  99.39%
Synonyms: CX-1632; S-47445
Target:  

iGluR mTOR

Research Areas:  

Neurological Disease

Tulrampator (S-47445) is an orally active selective AMPA receptor modulator. Tulrampator possesses procognitive, enhancing synaptic plasticity, anti-depressant-anxiolytic-like, procognitive and potential neuroprotective properties. Tulrampator can be used for research of alzheimer’s disease and in major depressive disorder .
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2
2 Cited Publications
Cat. No.: HY-10174
CAS No.: 212631-67-9
Purity:  98.08%
Target:  

MEK Apoptosis

Research Areas:  

Neurological Disease Cancer

PD184161 is an orally active MEK inhibitor. PD184161 inhibits MEK activity (IC50=10-100 nM) in a time- and concentration-dependent manner. PD184161 inhibits cell proliferation and induces apoptosis. PD184161 produces depressive-like behavior .
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2
2 Cited Publications
Cat. No.: HY-114452
CAS No.: 1307245-86-8
Purity:  99.91%
Synonyms: BTRX-246040
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

LY2940094 (BTRX-246040) is a potent, selective and orally available nociceptin receptor (NOP receptor) antagonist with high affinity (Ki=0.105 nM) and antagonist potency (Kb=0.166 nM). LY2940094 reduces ethanol self-administration in animal models .
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2
2 Cited Publications
Cat. No.: HY-114452A
CAS No.: 1307245-87-9
Synonyms: BTRX-246040 tartrate
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

LY2940094 (BTRX-246040) tartrate is a potent, brain penetrant, selective and orally available N/OFQ peptide (NOP) receptor antagonist with high affinity (Ki=0.105 nM) and antagonist potency (Kb=0.166 nM). LY2940094 tartrate reduces Ethanol self-administration and Ethanol seeking in animal models .
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2
2 Cited Publications
Cat. No.: HY-100769
CAS No.: 1339058-04-6
Purity:  99.73%
Synonyms: YL0919
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Hypidone hydrochloride (YL0919) is an orally active antidepressant agent with dual activity as a highly seletive 5-HT uptake blocker and an effective 5-HT1A receptor agonist (Ki=0.19 nM). Hypidone hydrochloride inhibits the uptake of [ 3H]-5-HT into rat cerebral cortical synaptosomes and HEK293 cells with IC50s of 1.78 nM and 1.93 nM, respectively. Hypidone hydrochloride shows remarkable antidepressant effects in animal models and has the poential for the investigation of depressive disorder .
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