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Signaling pathways

Items 1-10 of 5291

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  1. Calcipotriol monohydrate
    A3272 Calcipotriol monohydrate
    Summary: A synthetic vitamin D3 analogue
      ≥53.7 mg/mL
  2. Z-FY-CHO
    A9078 Z-FY-CHO
    Summary: Z-FY-CHO is a potent and specific cathepsin L inhibitor.
      ≥49.2 mg/mL
  3. Taurocholic acid-d4
    A9082 Taurocholic acid-d4
    Summary: Taurocholic acid-d4 is deuterium labeled Taurocholic acid. It intended for use as an internal standard for the quantification of TCA by GC- or LC-MS.
      Soluble in DMSO
  4. L-Cysteine-¹³C3
    A9083 L-Cysteine-¹³C3
    Summary: L-Cysteine-¹³C3 is the ¹³C-labeled L-Cysteine. It acts as a precursor for biologically active molecules such as hydrogen sulphide (H2S), glutathione and taurine. L-Cysteine suppresses ghrelin and reduces appetite in rodents and humans.
      Soluble in DMSO
  5. Taurolithocholic Acid MaxSpec® Standard
    A9076 Taurolithocholic Acid MaxSpec® Standard
    Summary: Taurolithocholic acid is a quantitative analytical standard guaranteed to meet MaxSpec identity, purity, stability, and concentration specifications.
      Soluble in DMSO
  6. Prostaglandin F2α ethanolamide
    A9077 Prostaglandin F2α ethanolamide
    Summary: Prostaglandin F2α ethanolamide is an ethanolamide-class G protein-coupled receptor (GPCR). It also acts as a luteolytic hormone in sheep and may serve as a nociceptive mediator in the spinal cord.
      Soluble in DMSO
  7. Androgen receptor antagonist 9
    A9989 Androgen receptor antagonist 9
    Summary: An Androgen receptor (AR) antagonist
      ≥52.4 mg/mL
  8. Warfarin sodium (Contains isopropyl alcohol)
    A9993 Warfarin sodium (Contains isopropyl alcohol)
    Summary: An effective anticoagulant agent
      ≥49.2 mg/mL
  9. Spermidine
    M1123 Spermidine
    Summary: Spermidine maintains cell membrane stability, increases antioxidant enzyme activity, and improves photosystem II (PSII) and related gene expression.
      ≥4 mg/mL
  10. Irpagratinib
    BA8948 Irpagratinib
    Summary: Irpagratinib (ABSK011) is an orally active inhibitor of fibroblast growth factor receptor (FGFR) tyrosine kinase, targeted (IC50<10nM).

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