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Results for "

PYR

" in MedChemExpress (MCE) Product Catalog:

22

Inhibitors & Agonists

2

Biochemical Assay Reagents

17

Peptides

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-13296
    PYR-41
    Maximum Cited Publications
    11 Publications Verification

    E1/E2/E3 Enzyme Apoptosis Cancer
    PYR-41 is a selective and cell permeable inhibitor of ubiquitin-activating enzyme E1 with an IC50 of < 10 μM, with little activity at E2 and E3.
    <em>PYR</em>-41
  • HY-153225

    HIV Infection
    PYR01 is a potent HIV-1 nonnucleoside reverse transcriptase inhibitor. PYR01 is an also targeted activator of cell kill molecules eliminate cells expressing HIV-1 .
    <em>PYR</em>01
  • HY-W010929

    Biochemical Assay Reagents Others
    PYR14-TFSI is a room temperature ionic liquid (RTIL) with a wide electrochemical window (5.5V) and a high viscosity, making it a useful candidate for electrochemical energy applications .
    <em>PYR</em>14-TFSI
  • HY-19408
    Pyr10
    3 Publications Verification

    TRP Channel Others
    Pyr10 is a pyrazole derivative and a selective TRP cation 3 (TRPC3) inhibitor. Pyr10 inhibits Ca 2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells with an IC50 of 0.72 μM (IC50 of 13.08 μM for store operated Ca 2+ entry in BRL-2H3 cells). Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels .
    <em>Pyr</em>10
  • HY-W009472

    PYR

    Fluorescent Dye Amino Acid Derivatives Others
    L-Pyroglutamic acid β-naphthylamide (PYR) is aglutamic acid derivatives.
    L-Pyroglutamic acid β-naphthylamide
  • HY-P2000

    (PYR6,Pro9)-Substance P

    Neurokinin Receptor Neurological Disease
    Septide ((Pyr6,Pro9)-Substance P) is a potent NK1 receptor agonist with a Kd value of 0.55 nM .
    Septide
  • HY-P4882

    Amyloid-β Neurological Disease
    (Pyr3)-Amyloid β-Protein (3-42) is the predominant amyloid β-peptide structure deposited in human brain of Alzheimer's disease and Down's syndrome patients. (Pyr3)-Amyloid β-Protein (3-42) is suggested to accumulate in the brain and to trigger the formation of insoluble amyloid β-peptide deposits .
    (<em>Pyr</em>3)-Amyloid β-Protein (3-42)
  • HY-108465
    Pyr3
    5+ Cited Publications

    TRP Channel Others
    Pyr3 is a selective inhibitor of transient receptor potential canonical channel 3 (TRPC3), with an IC50 of 700 nM for TRPC3-mediated Ca 2+ influx.
    <em>Pyr</em>3
  • HY-P4882A

    Amyloid-β Neurological Disease
    (Pyr3)-Amyloid β-Protein (3-42) TFA is the predominant amyloid β-peptide structure deposited in human brain of Alzheimer's disease and Down's syndrome patients. (Pyr3)-Amyloid β-Protein (3-42) TFA is suggested to accumulate in the brain and to trigger the formation of insoluble amyloid β-peptide deposits .
    (<em>Pyr</em>3)-Amyloid β-Protein (3-42) (TFA)
  • HY-12504
    Pyr6
    1 Publications Verification

    N-[4-[3,5-Bis(trifluoromethyl)-1H-PYRazol-1-yl]phenyl]-3-fluoro-4-PYRidinecarboxamide

    TRP Channel Others
    Pyr6 is a selective inhibitor of TRPC3 with IC50 of 0.49 uM(Ca2+ influx inhibition in thapsigargin depleted native RBL-2H3 cells).
    <em>Pyr</em>6
  • HY-118115

    Others Others
    Pyrabactin is a seed-selective abscisic acid (ABA) agonist that acts through Pyrabactin Resistance 1 (PYR1). Pyrabactin is used as a synthetic plant growth inhibitor .
    Pyrabactin
  • HY-107680

    3-PYR-Cyt

    nAChR Neurological Disease
    3-Pyr-Cytisine (3-Pyr-Cyt) is a cytisine derivative. 3-Pyr-Cytisine is a very weak α4β2 nAChR partial agonist that has been studied as an antidepressant .
    3-<em>Pyr</em>-Cytisine
  • HY-19735
    KJ Pyr 9
    5 Publications Verification

    c-Myc Autophagy Cancer
    KJ Pyr 9 is an inhibitor of MYC with a Kd of 6.5 nM in in vitro assay.
    KJ <em>Pyr</em> 9
  • HY-P1033
    [Pyr1]-Apelin-13
    1 Publications Verification

    [pGlu1]-Apelin-13

    Apelin Receptor (APJ) Cardiovascular Disease
    [Pyr1]-Apelin-13 is a highly potent, selective endogenous apelin receptor (APJ) agonist.
    [<em>Pyr</em>1]-Apelin-13
  • HY-W009673

    N-Boc-L-PYRoglutamic acid

    Biochemical Assay Reagents Others
    Boc-Pyr-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    Boc-<em>Pyr</em>-OH
  • HY-P4463

    GnRH Receptor Others
    (Des-Pyr1)-LHRH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
    (Des-<em>Pyr</em>1)-LHRH
  • HY-P4467

    (Des-PYR1)-Leuprolide

    GnRH Receptor Others
    (Des-Pyr1,Des-Gly10,D-Leu6,Pro-NHEt9)-LHRH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
    (Des-<em>Pyr</em>1,Des-Gly10,D-Leu6,Pro-NHEt9)-LHRH
  • HY-P4447

    GnRH Receptor Others
    (Des-Gly10,D-Pyr1,D-Leu6,Pro-NHEt9)-LHRH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
    (Des-Gly10,D-<em>Pyr</em>1,D-Leu6,Pro-NHEt9)-LHRH
  • HY-P2416

    Rat Gastrin-17

    Cholecystokinin Receptor Endocrinology
    Gastrin I, rat (Rat Gastrin-17) is a peptide hormone, can stimulate gastric acid secretion potently .
    Gastrin I, rat
  • HY-161063

    Dihydrofolate reductase (DHFR) Cancer
    DHFR-IN-14 (compound 32) is a pyrimethamine (Pyr)-type, dihydrofolate reductase (DHFR) inhibitor with potential anticancer activity .
    DHFR-IN-14
  • HY-139485

    Apelin Receptor (APJ) Cardiovascular Disease
    BMS-986224 is a potent, selective and orally active APJ receptor agonist (Kd = 0.3 nM). BMS-986224 exhibits similar receptor binding and signaling profile to (Pyr 1) apelin-13. BMS-986224 has the potential for the research of heart failure .
    BMS-986224
  • HY-B0439S1

    Sulphadoxine d3

    Parasite Antibiotic Infection
    Sulfadoxine-d3 is a deuterium labeled Sulfadoxine (HY-B0439). Sulfadoxine is a sulfonamide that is used, usually in combination with Pyrimethamine (HY-18062), for multidrug-resistant Plasmodium falciparum and P. vivax inhibition. Unlike PYR, Sulfadoxine has no impact on HIV replication or MT-2 cell cycle progression. But also Sulfadoxine exhibits suppression on respiratory, and urinary tract infections[1][2][3][4].
    Sulfadoxine D3

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