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Results for "

RD2

" in MedChemExpress (MCE) Product Catalog:

11

Inhibitors & Agonists

1

Natural
Products

1

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W007880

    (R)-Diphenylprolinol

    Drug Isomer Neurological Disease
    (R)-D2PM ((R)-Diphenylprolinol) is an isomer of the psychoactive substance D2PM and a pyrrolidine analog .
    (R)-D2PM
  • HY-N2516

    Others Inflammation/Immunology
    Ginsenoside Rd2 is a saponin found in Panax japonicus with anti-inflammatory actions .
    Ginsenoside Rd2
  • HY-14328

    PNU-101387G; U-101387G

    Dopamine Receptor Neurological Disease
    Sonepiprazole (PNU-101387G) is a selective D4 dopamine antagonist with Kis of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively .
    Sonepiprazole
  • HY-101065

    (+)-AJ 76 hydrochloride; (1S,2R)-AJ 76 hydrochloride

    Dopamine Receptor Others
    AJ-76 hydrochloride ((+)-AJ 76 hydrochloride) is an antagonist of dopamine autoreceptor with pKi values of 6.95, 6.67, 6.37, 6.21 and 6.07 for hD3, hD4, hD2S, hD2L and rD2 receptors, respectively.
    AJ-76 hydrochloride
  • HY-12442

    STAT Apoptosis Cancer
    LY5 is a STAT3 inhibitor with an IC50 value of 0.5 μM. LY5 induces apoptosis and inhibits STAT3 phosphorylation. LY5 shows antitumor activity in vivo, it can be used for the research of cancer .
    LY5
  • HY-W007880A

    (R)-Diphenylprolinol hydrochloride

    Drug Isomer Neurological Disease
    (R)-D2PM ((R)-Diphenylprolinol) hydrochloride is an isomer of the psychoactive substance D2PM and a pyrrolidine analog .
    (R)-D2PM hydrochloride
  • HY-123676

    PNU-101387G mesylate; U-101387G mesylate

    Dopamine Receptor Neurological Disease
    Sonepiprazole mesylate is a selective D4 dopamine antagonist with Kis of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively .
    Sonepiprazole mesylate
  • HY-14328A

    PNU-101387G hydrochloride; U-101387G hydrochloride

    Dopamine Receptor Neurological Disease
    Sonepiprazole (PNU-101387G) hydrochloride is a selective D4 dopamine antagonist with Kis of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively .
    Sonepiprazole hydrochloride
  • HY-RS11218

    Small Interfering RNA (siRNA) Others

    PRPH2 Human Pre-designed siRNA Set A contains three designed siRNAs for PRPH2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    PRPH2 Human Pre-designed siRNA Set A
    PRPH2 Human Pre-designed siRNA Set A
  • HY-175504

    Dopamine Receptor PERK 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 .
    MLS6357
  • HY-175532

    mAChR Neurological Disease
    M4 mAChR Modulator-2 is an orally active, selective, brain-penetrant positive allosteric modulator (PAM) of the M4 muscarinic acetylcholine receptor (M4 mAChR) (EC50 = 513 nM). M4 mAChR Modulator-2 exhibits high target selectivity, showing negligible affinity and low inhibition rates for non-target receptors (D1R/D2R/D3R, 5-HT subtypes, κ/δ/μ opioid receptors, H1, M1/M2) while specifically binding to M4 mAChR with a Ki of 377 nM and an inhibition rate of 62.8%. M4 mAChR Modulator-2 reverses Dizocilpine (MK-801) (HY-15084B)-induced hyperlocomotion in mice. M4 mAChR Modulator-2 can be used for the study of schizophrenia
    M4 mAChR Modulator-2

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