Other inhibitors

Items 851-900 of 980

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  1. E-982 is extracted from the reference, compound 12.
  2. fibrinogen receptor antagonist

    SC-52012 is an orally active fibrinogen receptor antagonist, with antiplatelet activities.

  3. memory-enhancing agent

    CL-275838 is a memory-enhancing agent, also with potent antidepressant activities.
  4. PEP inhibitor

    Z-321 is a prolylendopeptidase (PEP) inhibitor.
  5. KW-6055 is a benzylpyridine derivative and has anti-amnesic activity.
  6. Trombodipine is an antithrombotic agent.
  7. hypolipidemic agent

    TA-1801 is a hypolipidemic agent.
  8. Fenclozine is a non-steroidal antiinflammatory drug extracted from patent WO 2012112690 A2.
  9. Valrocemide (TV1901) is a promising antiepileptic drug candidate that shows a broad spectrum of anticonvulsant activity.
  10. FKK

    bronchodilator

    FKK is an indazole derivative and also a novel bronchodilator.
  11. 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.
  12. Cease inhibitor

    SMP-028 is an inhibitor of neutral cholesterol esterase (CEase), with an IC50 of 1.01 μM.
  13. LS2265 is a taurine derivative of fenofibrate and can induce proliferation of peroxisomes in liver cells of rats.
  14. hTGase inhibitor

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

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

    Voxelotor (GBT 440) is an orally bioavailable sickle hemoglobin (HbS) polymerization inhibitor.
  17. α-Tocopherol phosphate is the compound demonstrating the highest vitamin E activity, which is available both in its natural form as RRR-alpha-tocopherol isolated from plant sources.
  18. Glufosfamide is a novel alkylating agent in which the active metabolite of isophosphoramide mustard is glycosidically linked to β-D-glucose.
  19. PROTO-1 shows significant protection of hair cells, with HC50(concentration that would produce 50% hair cell survival) of 1 μM-10 μM (1 μM??HC50??10 μM).
  20. BoNTA LC inhibitor

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

    HQ-415 is a class of clinically relevant bioactive metal chelators related to clioquinol. The effective concentration eliciting a EC50 for HQ-415 is 15 μM.
  22. SAHH inhibitor

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

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

    HLM006474 is a pan E2F inhibitor, which inhibits E2F4 DNA-binding with an IC50 of 29.8 ?M in A375 cells.
  25. 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.
  26. 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.
  27. 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.
  28. PIP5K1α inhibitor

    ISA-2011B is a PIP5Kα inhibitor with promising anticancer effects .
  29. 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.
  30. (R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (ISF 2522) is a nootropic drug of the racetam family and stimulant.
  31. Vitamin CK3 is the combination of Vitamin C and vitamin K3 (100:1 ratio) and has been shown to inhibit tumor growth and lung metastasis.
  32. RR6

    vanin inhibitor

    RR6 is a selective, reversible, and competitive vanin inhibitor.
  33. Furilazole(MON-13900) is a pesticide agent.
  34. Antitumor agent-3 is a potent compound which comprises a new imidazopyridine having excellent antitumor activity as an active ingredient.
  35. Chromafenozide (ANS118) is a lepidopteran insecticide; it is highly effective in controlling various lepidopteran pests.
  36. plant growth regulator

    Cloxyfonac is a plant growth regulator and a chemical transformation product; Pesticide agent.
  37. Benoxafos (HOE 2910) is an insecticide.
  38. Athidathion(GS-13006) is an organophosphate insecticide.
  39. Cobalt phthalocyanine is a catalyst of redox reaction, catalyzes aerobic regenerations of aldehydes and ketones from aldoximes and ketoximes has been developed.
  40. Novaluron is a chemical with pesticide properties, belonging to the class of insecticides called insect growth regulators.
  41. Ipfencarbazone is a substance being developed for the control of weeds such as watergrass in rice; herbicide agent.
  42. Ropidoxuridine (IPdR) is a novel orally available, halogenated thymidine analog and is a potential radiosensitizer for use in human tumors.
  43. RH1
    RH1 (NSC 697726) is a potent bioreductive agent with profound anti-cancer activity in vitro and in vivo.
  44. DβH inhibitor

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

    PSI-697 is an oral P-selectin inhibitor with an IC50 of 125 μM.
  46. (R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid is a constrained Phe analogue which can fold into a beta-bend and a helical structure, and to adopt a preferred side-chain disposition in the peptide.
  47. 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.
  48. S186 is a kind of sodium salts of calcium-acetylpropylamine phosphonate(APA); a new strontium-specific chelating agent.
  49. 20-Hydroxyeicosatetraenoic acid synthesis inhibitor

    TS-011 is a selective inhibitor of 20-Hydroxyeicosatetraenoic acid synthesis.
  50. CHAPS is a zwitterionic nondenaturing detergent for solubilizing membrane proteins.

Items 851-900 of 980

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