9 Results for "

D5R

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "D5R" in MCE Product Catalog:

Art. -Nr.: HY-169116
Target:  

Dopamine Receptor

Forschungsgebiete:  

Neurological Disease

D5R agonist 1 (Compound 5j) is a selective, orally active and BBB penetrable D5R partial agonist (EC50: 269.7 nM). D5R agonist 1 enhances the cognition in the Scopolamine (HY-N0296)-induced amnesia model .
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Art. -Nr.: HY-175504
CAS. Nr.: 932544-59-7
Target:  

Dopamine Receptor PERK

Forschungsgebiete:  

Neurological Disease

MLS6357 is a D3 dopamine receptor (D3R)-selective positive allosteric modulator (PAM)-antagonist. MLS6357 exhibits antagonist activity in the D3R-mediated and the BRET-based β-arrestin recruitment assay with IC50s of 13 and 14 μM, and no activity for other DAR subtypes (D1R/D2R/D4R/D5R) (IC50 > 100 μM). MLS6357 is also an antagonist in the D3R-mediated Go-BRET assay with an IC50 of 17 μM. MLS6357 can be used for the study of neuropsychiatric disorders, including substance use disorder .
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Art. -Nr.: HY-18259
CAS. Nr.: 773852-25-8
Forschungsgebiete:  

Cancer

103D5R (Compound 15) is an inhibitor for the activation of hypoxia-inducible factor-1 (HIF-1) with an IC50 of 35 µM, through reduction of the HIF-1α protein synthesis. 103D5R inhibits the proliferation of LN229 with IC50 of 26 µM .
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Art. -Nr.: HY-152678
Forschungsgebiete:  

Cancer

6-Methoxypurine-9-β-D-5’(R)-C-methylriboside is a hypoxanthine analog. Hypoxanthine is a kind of purine base mainly present in muscle tissue. And it is a metabolite produced by purine oxidase acting on xanthine. Hypoxanthine has typical anti-inflammatory effects and is a potential endogenous poly(ADP-ribose) polymerase (PARP) inhibitor. It is cytoprotective by inhibiting PAPR activity, inhibiting peroxynitrite-induced mitochondrial depolarization and secondary superoxide production. Hypoxanthine can also be used as an indicator of hypoxia .
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Art. -Nr.: HY-RS04007
Forschungsgebiete:  

Others

Drd5 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Drd5 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-17385S
Synonyms: Tomoxetine-d5 hydrochloride; LY 139603-d5 ; (R)-Tomoxetine-d5 hydrochloride
Atomoxetine-d5 (hydrochloride) is the deuterium labeled Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively) .
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Art. -Nr.: HY-W738480
CAS. Nr.: 1177315-89-7
Synonyms: (R)-Tert-Butyl 2-amino-3-phenylpropanoate-d5
L-Phenylalanine tert-butyl ester-d5 ((R)-Tert-Butyl 2-amino-3-phenylpropanoate-d5) is the deuterium labeled (S)-tert-Butyl 2-amino-3-phenylpropanoate (HY-W108426).
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Art. -Nr.: HY-W704363
CAS. Nr.: 1794979-08-0
Synonyms: R6238-d5
Pimozide-d5 (R6238-d5) is the deuterium labeled Pimozide (HY-12987). Pimozide is a dopamine receptor antagonist, with Kis of 1.4 nM, 2.5 nM and 588 nM for dopamine D2, D3 and D1 receptors, respectively, and also has affinity at α1-adrenoceptor, with a Ki of 39 nM; Pimozide also inhibits STAT3 and STAT5.
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Art. -Nr.: HY-125527AS
Synonyms: 17(R)-RvD1-d5; AT-RvD1-d5
17(R)-Resolvin D1-d5 (17(R)-RvD1-d5) is deuterium labeled 17(R)-Resolvin D1. 17R-Resolvin D1 (17R-RvD1; AT-RvD1) is an aspirin-triggered epimer of Resolvin D1, which exhibits anti-inflammatory activity in mice and human PMNs cells . 17R-Resolvin D1 specificially inhibits TRPV3 with an IC50 of 398 nM and exhibits peripheral anti-nociceptive efficacy .
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