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  1. UGT1A1 substrate

    UK-157147 is a substrate for UDP-glucuronosyltransferases (UGT1A1) with a Km value of 105 μM.
  2. Gastrofensin AN 5 free base, a 4-phenyl-tetrahydroisoquinoline derivative, is an antiulcer agent.
  3. Sulfo-NHS-Biotin is an amine-reactive biotinylation reagent.
  4. Diflumidone is a non-steroidal antiinflammatory drug.
  5. RTC-30 is an optimized phenothiazine with anti-cancer potency. RTC-30 contains a hydroxylated linker (N) that confers increased oral bioavailability.
  6. KMO inhibitor

    GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor with IC50s of 2.3 nM and 0.7 nM for human KMO and P. fluorescens-KMO (Pf-KMO), respectively.
  7. Macropa-NH2 is the precursor of Macropa-NCS. Macropa-NCS is conjugated to trastuzumab as well as to the prostate-specific membrane antigen-targeting compound RPS-070 and is a promising therapeutic radionuclide applied in the treatment of soft-tissue metastases.
  8. MTPPA is a drug for treating symptoms of inflammation and pain.
  9. MDL 19301 is a nonsteroidal, anti-inflammatory agent.
  10. Y-9738 is a hypolipidemic agent.
  11. Fenclozine is a non-steroidal antiinflammatory drug extracted from patent WO 2012112690 A2.
  12. MBC-11 trisodium is a first-in-class conjugate of the bone-targeting bisphosphonate HEDP covalently linked to the antimetabolite Ara-C. Has potential to treat tumor-induced bone disease (TIBD).
  13. MSI-1701 is an analogue of MSI-1436 which can control weight gain and blood glucose level extracted from patent US 7410959 B1.
  14. anti-infective agent

    RGW 611, a morpholine derivative, is an impurity of Nimorazole, which is an anti-infective agent against anaerobic bacteria and protozoa.
  15. Thiambutosine was a candidate for treatment of lepromatous leprosy.

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