Other inhibitors

Shop By

Items 101-150 of 218

Page
per page
Set Descending Direction
Catalog No.
Product Name
Application
Product Information
Citations
  1. inhibitor for GA perception

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

    Ehp inhibitor 2 is a Eph family tyrosine kinase inhibitor.
  3. 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.
  4. 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).
  5. AKR1C3 inhibitor

    Stylopine is a potent AKR1C3 inhibitor.
  6. 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).
  7. IGPS inhibitor

    ATB107 is a novel and potent inhibitor of indole-3-glycerol phosphate synthase (IGPS) with a KD of 3 μM.
  8. FOXM1 inhibitor

    RCM-1 is a FOXM1 inhibitor.
  9. breast cancer stem cells inhibitor

    ML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM.
  10. nitrification inhibitor

    3-Methylpyrazole is used as a nitrification inhibitor of nitrification in soil.
  11. p18 inhibitor

    NSC23005 sodium is a novel and effective p18 inhibitor (ED50=5.21 nM) in promoting Hematopoietic stem cells (HSCs) expansion in both murine and human models.
  12. PCA-1/ALKBH3 inhibitor

    HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo.
  13. PEP inhibitor

    Z-321 is a prolylendopeptidase (PEP) inhibitor.
  14. glycogen phosphorylase inhibitor

    Ingliforib is a glycogen phosphorylase inhibitor, with IC50s of 52, 352 and 150 nM for liver, muscle and brain glycogen phosphorylase, and has cardioprotective activity.
  15. Cease inhibitor

    SMP-028 is an inhibitor of neutral cholesterol esterase (CEase), with an IC50 of 1.01 μM.
  16. hTGase inhibitor

    LDN-27219 is a potent inhibitor of hTGase(Tissue transglutaminase) with an IC50 of 0.6 uM.
  17. squalene synthase inhibitor

    Lapaquistat acetate (TAK-475) is a squalene synthase inhibitor, blocking the conversion of farnesyl diphosphate (FPP) to squalene.
  18. HbS polymerization inhibitor

    Voxelotor (GBT 440) is an orally bioavailable sickle hemoglobin (HbS) polymerization inhibitor.
  19. BoNTA LC inhibitor

    BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (BoNTA LC) with IC50 of 0.9 uM.
  20. SAHH inhibitor

    DZ2002 is a potent and reversible S-Adenosyl-L-homocysteine Hydrolase(SAHH; AdoHcy Hydrolase) inhibitor with Ki of 17.9 nM.
  21. α-glucoside hydrolase inhibitor

    Emiglitate (BAY o 1248) is a potent, selective and competitive inhibitor of α-glucoside hydrolase.
  22. E2F inhibitor

    HLM006474 is a pan E2F inhibitor, which inhibits E2F4 DNA-binding with an IC50 of 29.8 ?M in A375 cells.
  23. TrioN inhibitor

    ITX3 is a specific and nontoxic inhibitor of the TrioN (N-terminal GEF domain of the multidomain Trio protein) with IC50 of 76 uM; inhibits TrioN-stimulated RhoG exchange in vitro.
  24. insect chitinase and N- acetyl hexosaminidase inhibitor

    Chitinase-IN-2 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 μM/20 μM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively.
  25. insect chitinase and N- acetyl hexosaminidase inhibitor

    Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20 uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively.
  26. PIP5K1α inhibitor

    ISA-2011B is a PIP5Kα inhibitor with promising anticancer effects .
  27. FPPS inhibitor

    NE 10790, a poor farnesyl pyrophosphate synthase inhibitor, is a phosphonocarboxylate analogue of the potent bisphosphonate risedronate and is a weak antiresorptive agent.
  28. RR6

    vanin inhibitor

    RR6 is a selective, reversible, and competitive vanin inhibitor.
  29. DβH inhibitor

    Etamicastat (BIA 5-453) is a potent and reversible peripheral dopamine-β-hydroxylase (DβH) inhibitor.
  30. P-selectin inhibitor

    PSI-697 is an oral P-selectin inhibitor with an IC50 of 125 μM.
  31. HO inhibitor

    Tin(IV) mesoporphyrin IX dichloride (Stannsoporfin) is a heme oxygenase (HO) inhibitor being developed for the prevention of hyperbilirubinemia in infants at risk of developing jaundice, extracted from patent WO2011103196A1.
  32. 20-Hydroxyeicosatetraenoic acid synthesis inhibitor

    TS-011 is a selective inhibitor of 20-Hydroxyeicosatetraenoic acid synthesis.
  33. KMO inhibitor

    UPF-648 is a potent kynurenine 3-monooxygenase (KMO) inhibitor; exhibits highly active at 1 uM (81 ?? 10% KMO inhibition); ineffective at blocking KAT activity.
  34. photosynthetic electron transport inhibitor

    Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.
  35. uricase inhibitor

    Potassium oxonate is an inhibitor of uricase, inhibits the phosphorylation of 5-FU to 5-fluorouridine-5'-monophosphate catalyzed by pyrimidine phosphoribosyl-transferase in a different manner from allopurinol in cell-free extracts and intact cells in vitro.
  36. PIK3C3/Vps34 inhibitor

    SAR405 R enantiomer is the less active enantiomer of SAR405. SAR405 is a PIK3C3/Vps34 inhibitor.
  37. neurotoxin inhibitor

    Neurotoxin Inhibitor is a neurotoxin inhibitor.
  38. FOXM1 inhibitor

    FDI-6 is an inhibitor of FOXM1. FDI-6 binds directly to FOXM1 protein, to displace FOXM1 from genomic targets in MCF-7 breast cancer cells, and induce concomitant transcriptional down-regulation.
  39. protease inhibitor

    N-alpha-Tosyl-L-lysine chloromethyl ketone (TLCK), a trypsin like protease inhibitor, sensitizes HeLa cells to Fas-mediated cell death.
  40. SMS2 inhibitor

    SMS2-IN-2 is a potent, highly selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, with IC50s of 100 nM and 56 μM for SMS2 and SMS1, respectively. Anti-chronic inflammatory activity.
  41. TAFIa inhibitor

    DS-1040 Tosylate is an inhibitor of the activated thrombin-activatable fibrinolysis inhibitor (TAFIa), used for the treatment of acute ischemic stroke (AIS).
  42. GLUD1 inhibitor

    R162 is a potent inhibitor of glutamate dehydrogenase 1 (GDH1/GLUD1), with anti-cancer properties.
  43. MRK inhibitor

    M443 is an irreversible and specific inhibitor of MRK, with an IC50<125 nM.
  44. HNE inhibitor

    BAY-677 is an inactive control for BAY-678. BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophil elastase (HNE), with an IC50 of 20 nM.
  45. anandamide transport inhibitor

    ARN272 is an anandamide transport inhibitor.
  46. TNP

    IP6K1/IP3K inhibitor

    TNP is a cell-permeable inhibitor of IP6K1 and IP3K, with IC50 values of 0.55 ?M and 10.2 ?M for IP3K, respectively. TNP binds to the ATP-binding sites of both enzymes.
  47. ACMSD inhibitor

    TES-991 is a potent and selective human α?Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD) inhibitor, with an IC50 of 3 nM.
  48. KMO inhibitor

    GSK180 is a selective, competitive, and potent inhibitor of kynurenine-3-monooxygenase (KMO), a key enzyme of tryptophan metabolism (IC50, ~6 nM), but shows negligible activity against other enzymes on the tryptophan pathway.
  49. Tx synthetase inhibitor

    Ro 22-3581 (4'-(Imidazol-1-yl) acetophenone) is a selective thromboxane (Tx) synthetase inhibitor.
  50. HO-1 inhibitor

    HO-1-IN-1 (Compound 2) is a heme oxygenase 1 (HO-1) inhibitor with an IC50 of 250 nM.

Items 101-150 of 218

Page
per page
Set Descending Direction