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Bioactive Compounds

Items 7711-7720 of 13157

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  1. L-741,742 hydrochloride
    B5044 L-741,742 hydrochloride
    Summary: highly potent and selective D4 dopamine receptor antagonist
      insoluble in DMSO
  2. Clemizole hydrochloride
    A3316 Clemizole hydrochloride
    Target: Histamine H1 Receptors|TRPC channel
    Summary: H1 histamine receptor antagonist
  3. Levobunolol hydrochloride
    A9987 Levobunolol hydrochloride
    Summary: A potent, non-selective β-adrenergic receptor antagonist
      Soluble in DMSO
  4. Melatonin-d4
    SL1035 Melatonin-d4
    Summary: A stable isotope deuterated compound of Melatonin
  5. Psychosine
    C3371 Psychosine
    Summary: A natural substrate of GALC, induces apoptosis and inhibits PKC activity.
      ≤1 mg/mL
  6. NRX-252262
    BA9140 NRX-252262
    Summary: NRX-252262 is a potent interaction enhancer with homologous SCF.
  7. Fmoc-Gly-Gly-Phe-OtBu
    BA2613 Fmoc-Gly-Gly-Phe-OtBu
    Summary: A commonly used degradable (cleavable) linker for antibody-coupled reactive molecules (ADCs).
  8. FT709
    BA3887 FT709
    Summary: FT709 is a potent and selective inhibitor.
  9. Tubacin
    A4501 Tubacin
     3 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC6 inhibitor,potent,selective,reversible,cell-permeable
      insoluble in EtOH; insoluble in H2O; ≥7.19 mg/mL
  10. SD 1008
    A4515 SD 1008
    Summary: Inhibitor of JAK2/STAT3 signaling pathway,apoptosis inducer
      <32.94 mg/mL

Items 7711-7720 of 13157

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