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Results for "

(R,R)-enantiomer

" in MedChemExpress (MCE) Product Catalog:

12

Inhibitors & Agonists

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-111532
    (3R,4R)-A2-32-01
    2 Publications Verification

    		 ClpP Bacterial Infection
    (3R,4R)-A2-32-01 (compound 24(R,R)), the (R,R)-enantiomer of A2-32-01, is a Staphylococcus aureus caseinolytic protease (SaClpP) inhibitor .
    (3R,4R)-A2-32-01
  • HY-169761B
    (R,R)-dWIZ-1 TFA

    		Molecular Glues Histone Acetyltransferase Cardiovascular Disease
    (R,R)-dWIZ-1 TFA is the the (R,R)-enantiomer of dWIZ-1 (HY-159098). dWIZ-1 is a potent WIZ molecular glue degrader. dWIZ-1 has the potential for the research of sickle cell disease (SCD) .
    (R,R)-dWIZ-1 TFA
  • HY-B0010D
    Arformoterol tartrate
    1 Publications Verification

    (R,R)-Formoterol tartrate

    		 Adrenergic Receptor Inflammation/Immunology
    Arformoterol ((R,R)-Formoterol) tartrate, the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol tartrate can be used for the research of chronic obstructive pulmonary disease (COPD) .
    Arformoterol tartrate
  • HY-B0010A
    Arformoterol
    1 Publications Verification

    (R,R)-Formoterol

    		 Adrenergic Receptor Inflammation/Immunology
    Arformoterol ((R,R)-Formoterol), the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol can be used for the research of chronic obstructive pulmonary disease (COPD) .
    Arformoterol
  • HY-B0010AS
    Formoterol-d3

    		Isotope-Labeled Compounds Adrenergic Receptor Inflammation/Immunology
    Formoterol-d3 is deuterium labeled Arformoterol. Arformoterol ((R,R)-Formoterol), the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol can be used for the research of chronic obstructive pulmonary disease (COPD) .
    Formoterol-d3
  • HY-149318B
    (R,R)-VRT-534

    		Connexin Gap Junction Protein Others
    (R,R)-VRT-534 is the (R,R)-enantiomer of VRT-534 (HY-149318). VRT-534 (Compound 3) is a chemical chaperone targeting connexin 26 (Cx26). Vrt-534 exhibits dose-responsive binding to recombinant WT Cx26 and mutant Cx26 K188N with EC50s of 19 and 5 μM, respectively. Vrt-534 can be used in research related to hearing impairment .
    (R,R)-VRT-534
  • HY-17423I
    (R,R)-Abacavir

    		HIV Reverse Transcriptase Telomerase Apoptosis Drug Isomer Infection Cancer
    (R,R)-Abacavir is the (R,R)-enantiomer of Abacavir (HY-17423). Abacavir is an orally active and competitive nucleoside reverse transcriptase inhibitor. Abacavir can inhibits the replication of HIV. Abacavir shows anticancer activity in prostate cancer cell lines. Abacavir can trespass the blood-brain-barrier and suppresses telomerase activity .
    (R,R)-Abacavir
  • HY-153321A
    (R,R)-Bexobrutideg

    (R,R)-NX-5948; (R,R)-BTK-IN-24

    		 Drug Isomer PROTACs Btk Inflammation/Immunology Cancer
    (R,R)-Bexobrutideg is the (R,R)-enantiomer of Bexobrutideg (HY-153321). Bexobrutideg (NX-5948) is an orally active PROTAC that induces specific BTK protein degradation via a cereblon E3 ligase (CRBN) complex without degrading other cereblon neo substrates. Bexobrutideg mediates potent anti-inflammatory activity through BTK degradation, thereby inhibiting B cell activation. Bexobrutideg exhibits potent tumor growth inhibition in TMD8 xenograft models containing wild-type BTK or BTKi resistance mutations. Bexobrutideg is effective in a mouse model of collagen-induced arthritis (CIA). Bexobrutideg can cross the blood-brain barrier. NX-5948 consists of a target protein ligand, a linker, and a VHL E3 ubiquitin ligase (Red: BTK ligand (HY-170324); Blue: CRBN ligand (HY-171893); Black: linker) .
    (R,R)-Bexobrutideg
  • HY-W018061C
    (R,R)-Traxoprodil

    (R,R)-CP101,606

    		 iGluR Neurological Disease
    (R,R)-Traxoprodil is the the (R,R)-enantiomer of Traxoprodil (HY-W018061). Traxoprodil (CP101,606) is a potent and selective NMDA antagonist and protect hippocampal neurons with an IC50 of 10 nM .
    (R,R)-Traxoprodil
  • HY-B0010E
    Arformoterol maleate

    (R,R)-Formoterol maleate

    		 Adrenergic Receptor Inflammation/Immunology
    Arformoterol ((R,R)-Formoterol) maleate, the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol maleate can be used for the research of chronic obstructive pulmonary disease (COPD) .
    Arformoterol maleate
  • HY-B0010DR
    Arformoterol tartrate (Standard)

    (R,R)-Formoterol tartrate (Standard)

    		 Reference Standards Adrenergic Receptor Inflammation/Immunology
    Arformoterol (tartrate) (Standard) is the analytical standard of Arformoterol (tartrate). This product is intended for research and analytical applications. Arformoterol ((R,R)-Formoterol) tartrate, the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol tartrate can be used for the research of chronic obstructive pulmonary disease (COPD) .
    Arformoterol tartrate (Standard)
  • HY-152092A
    (R,R)-MMP-1-IN-1

    		Drug Isomer Others
    (R,R)-MMP-1-IN-1 is the R,R-enantiomer of MMP-1-IN-1 (HY-152092). MMP-1-IN-1 (Compound 6) is a highly potent MMP-1 inhibitor with an IC50 of 0.034 μM .
    (R,R)-MMP-1-IN-1

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