71 Results for "

OX2-R

" in MedChemExpress (MCE) Product Catalog:
Products (71)

71 Results for "OX2-R" in MCE Product Catalog:

Cat. No.: HY-162235
CAS No.: 1803557-42-7
Research Areas:  

Cardiovascular Disease

CVN766 is an orally active inhibitor of orexin 1 receptor antagonist with blood-brain permeability with the IC50 values of 8 nM and >10 μM for OX1R and OX2R, respectively. CVN766 can be used for study schizophrenia .
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Cat. No.: HY-147403S
CAS No.: 1637681-55-0
Synonyms: JNJ-61393215
Tebideutorexant is an OX1R-selective inhibitor with oral bioavailability and blood-brain barrier permeability, with human OX1R pKi 8.17 and rat OX1R pKi 8.13.Tebideutorexant selectively modulates OX1R, with no significant functional effect on OX2R. Tebideutorexant can be used for the research of panic and anxiety disorders .
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Cat. No.: HY-137452
CAS No.: 2274802-89-8
Purity:  98.66%
Research Areas:  

Neurological Disease

Suntinorexton is an OX2R agonist. Suntinorexton is used to study respiratory function during sleep .
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Cat. No.: HY-137440
CAS No.: 2274802-95-6
Purity:  99.94%
Synonyms: TAK-994 free base
Research Areas:  

Neurological Disease

Firazorexton (TAK-994 free base) is an orally active and brain-penetrant orexin type 2 receptor (OX2R) selective agonist. Firazorexton (TAK-994 free base) can promote wakefulness and has the potential to improve narcolepsy-like symptoms in mice .
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Cat. No.: HY-177096
CAS No.: 2758363-88-9
Research Areas:  

Neurological Disease

Ledasorexton is an orally active OX2R agonist (EC50: 0.99 nM). Ledasorexton has awakening effect in mice. Ledasorexton can be used for research of neurological disease .
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Cat. No.: HY-177073
CAS No.: 2980518-93-0
Cleminorexton is an orally active orexin-2 receptor (OX2R) agonist with a pEC50 between 9 and 10.4. Cleminorexton can be used for narcolepsy and other conditions associated with orexin deficiency and/or excessive sleepiness .
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Cat. No.: HY-12301
CAS No.: 1224846-01-8
Purity:  98.83%
Research Areas:  

Neurological Disease

MK-3697 is an orally active orexin 2 receptor (OX2R) antagonist, with an IC50 value of 16 nM and a Ki value of 1.1 nM against human OX2R. MK-3697 blocks the wake-promoting OX2R signaling pathway, reduces active wake time, and increases slow-wave sleep and rapid eye movement sleep time in mice, rats and dogs. MK-3697 can be used for research on insomnia .
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Cat. No.: HY-N7325
CAS No.: 29505-31-5
Valerosidate is an OX2R antagonist. Valerosidate increases expression of tumor suppressor proteins p53 and PTEN, selectively reduces colon cancer cell viability, and suppresses colon cancer cell migration. Valerosidate can be used for the research of colon cancer and insomnia [2].
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Cat. No.: HY-RS06054
Research Areas:  

Others

HCRTR2 Human Pre-designed siRNA Set A contains three designed siRNAs for HCRTR2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-100452A
CAS No.: 1610882-30-8
Synonyms: OX2R antagonist
Research Areas:  

Endocrinology Cancer

TCS-OX2-29 (hydrochloride) is a potent, high affinities and selective orexin-2 receptor (OX2R) antagonist with an IC50 value of 40 nM and a pKI value of 7.5. TCS-OX2-29 displays ~250-fold selectivity for OX2 over OX1 [2].
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Cat. No.: HY-162712
CAS No.: 2460722-03-4
OX-201 is an orally active, blood-brain barrier-permeable OX2R agonist with an EC50 of 8.0 nM. OX-201 activates OX2R to induce wakefulness and neuronal activation. OX-201 promotes the release of neuron activity-dependent tau protein from neurons into the interstitial fluid of hippocampal tissues. OX-201 is applicable to research related to Alzheimer's disease and tauopathies .
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Cat. No.: HY-178871
CAS No.: 1607428-33-0
Research Areas:  

Neurological Disease

OX2-2303 is a potent, selective orexin-2 receptor (OX2R) antagonist. OX2-2303 exhibits excellent binding affinity towards OX2R (Ki = 0.1 nM), and shows >890-fold selectivity over OX1R. OX2-2303 can be used as a positron emission tomography (PET) radioligand for central nervous system (CNS) research .
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Cat. No.: HY-177085
CAS No.: 2839408-03-4
Research Areas:  

Neurological Disease

Fumiporexant (Compound Example 93) is an orally active, brain-penetrant and selective Orexin receptor 2 (OX2R) antagonist. Fumiporexant regulates the sleep-wake cycle and emotion-related pathways in the central nervous system. Fumiporexant is promising for research of nervous system diseases such as insomnia and major depressive disorder .
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Cat. No.: HY-159731
CAS No.: 2648347-78-6
Research Areas:  

Neurological Disease

OX2R agonist 1 is an OX2R antagonist with an EC50 of less than 100 nM. OX2R agonist 1 can be used in research related to excessive daytime sleepiness or narcolepsy .
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Cat. No.: HY-163276
Research Areas:  

Neurological Disease

OX2R agonist 3 (compound 63c) is an agonist for orexin receptor type 2 (OX2R) with EC50 of 339 nM. OX2R agonist 3 is able to cross the blood-brain barrier and exhibits no cytotoxicity in cells
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Cat. No.: HY-RS18434
Research Areas:  

Others

Cd200r1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cd200r1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-149014
CAS No.: 2639148-08-4
Research Areas:  

Neurological Disease

OX2R-IN-1 (compound 15) is a low cytotoxicity profile OX2R-IN-1 antagonist (a potential OX2R binder) with an IC50 value of 484 μM. OX2R-IN-1 (compound 15) can cross the BBB into the brain with a short half-life .
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Cat. No.: HY-146517
CAS No.: 2251017-69-1
Research Areas:  

Neurological Disease

Orexin receptor antagonist 4 is potent and selective orexin 2 receptor (OX2R) antagonist with an IC50 of 4.27 nM. Orexin receptor antagonist 4 is 61-fold selective for the OX2R over the OX1R (IC50 of 295 nM) (WO2018206959A1; example 1) .
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Cat. No.: HY-161567
CAS No.: 2791360-37-5
Research Areas:  

Neurological Disease

OX2R-IN-3 (Compound 53) is an orally active type 2 orexin receptor (OX2R) agonist (EC50<100 nM.) .
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Cat. No.: HY-171032B
CAS No.: 2923137-99-7
Research Areas:  

Neurological Disease

YNT-3708 is an orexin receptor (OXR) agonist, with EC50 values of 14.6 nM and 277 nm for OX1R and OX2R, respectively .
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