Other inhibitors

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  1. triazole DAGL(α) inhibitor

    DO34 analog is a triazole DAGL(α) inhibitor extracted from patent WO2017096315 A1, compound 100.
  2. enkephalin degrading enzymes inhibitor

    Kelatorphan is a full inhibitor of enkephalin degrading enzymes.
  3. CDC7 kinase inhibitor

    (R)-Simurosertib ((R)-TAK-931) is the (R)-enantiomer of Simurosertib, Simurosertib (TAK-931) is a selective cycle 7 (CDC7) kinase inhibitor, with an IC50<0.3 nM.
  4. SAMDC inhibitor

    Sardomozide is an S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM.
  5. VP40 Inhibitor

    ASN03576800 is an inhibitor of the VP40 matrix protein.
  6. Ces3 inhibitor

    WWL229 is a selective inhibitor of Ces3 that acts by inhibiting recombinant Ces3 and recapitulating the effects of WWL113 in adipocytes.
  7. polymerase inhibitor

    ERDRP-0519 is an orally available inhibitor of polymerase that shows efficacy against a lethal morbillivirus infection in a large animal model.
  8. p18INK inhibitor

    NSC23005 is a p18INK inhibitor. NSC23005 potently promotes hematopoietic stem cell (HSC) expansion (ED50 = 5.21 nM).
  9. 3CLpro inhibitor

    GC376 is a 3CLpro inhibitor (3C-like protease inhibitor).
  10. inhibitor for GA perception

    TSPC is an inhibitor for GA perception by in vitro and in planta evaluations.
  11. Eph family tyrosine kinase inhibitor

    Ehp inhibitor 2 is a Eph family tyrosine kinase inhibitor.
  12. S-adenosylhomocysteine hydrolase inhibitor

    3-Deazaadenosine (hydrochloride) is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 ?M; 3-Deazaadenosine has anti-inflammatory, anti-proliferative and anti-HIV activity.
  13. inhibitor of glycogen synthase kinase 3

    5-bromoindole is an important pharmaceutical chemical intermediate and a potential inhibitor of glycogen synthase kinase 3 (GSK-3).
  14. AKR1C3 inhibitor

    Stylopine is a potent AKR1C3 inhibitor.
  15. PLAP inhibitor

    ML-095 is an inhibitor of PLAP (IC50 = 3.7 μM) that demonstrates high selectivity against the related alkaline phosphatases, TNAP and IAP (IC50s > 100 μM).
  16. transcriptional inhibitor of G0/G1 switch 2

    NS-3-008 hydrochloride is an orally active transcriptional inhibitor of G0/G1 switch 2 (G0s2) with an IC50 of 2.25 μM. NS-3-008 hydrochloride can be used for chronic kidney disease.
  17. chemical cyclophilin A inhibitor

    TMN355 is a potent chemical cyclophilin A inhibitor and reduces foam cell formation and cytokine secretion. TMN355 is used for atherosclerosis.

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