Other inhibitors

Items 551-600 of 980

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  1. non-narcotic analgesic

    Simetride, a non-narcotic analgesic, is an ingredient of Kyorin AP2 which is used to treat low back pain, symptomatic neuralgia, headache, menstrual pain and etc.
  2. antilipidemic agent

    Nicomol is a niacin derivative that exhibits antilipidemic activity.
  3. p18INK inhibitor

    NSC23005 is a p18INK inhibitor. NSC23005 potently promotes hematopoietic stem cell (HSC) expansion (ED50 = 5.21 nM).
  4. Thiambutosine was a candidate for treatment of lepromatous leprosy.
  5. Isocyclosporin A is a rearranged degradation product formed by acid treatment of cyclosporin A under aqueous and non-aqueous conditions.
  6. Dextromethorphan (Discontinued) (DXM or DM) is an antitussive (cough suppressant) drug of the morphinan class with sedative and dissociative properties.
  7. inhibitor for GA perception

    TSPC is an inhibitor for GA perception by in vitro and in planta evaluations.
  8. autoinducer of P. fischeri luciferase

    N-(beta-ketocaproyl)-L-Homoserine lactone (N-(Ketocaproyl)-L-homoserine lactone, N-(β-Ketocaproyl)-L-hoMoserine lactone) is an autoinducer of P. fischeri luciferase and a component of quorum regulatory sensing.
  9. Eph family tyrosine kinase inhibitor

    Ehp inhibitor 2 is a Eph family tyrosine kinase inhibitor.
  10. 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.
  11. antiproliferative agent

    Coumarin-3-carboxylic acid (2- Oxochromene-3-carboxylic acid) is an important initial compound for the synthesis of coumarins which are well known natural products for their diverse biological activities. Lanthanide complexes of Coumarin-3-carboxylic acid exhibit antiproliferative activity towards K-562 cell line.
  12. 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).
  13. non-steroidal anti-inflammatory drug

    Indoprofen is a non-steroidal anti-inflammatory drug, provide insight into treatments for spinal muscular atrophies.
  14. AKR1C3 inhibitor

    Stylopine is a potent AKR1C3 inhibitor.
  15. Violanthrone-79 is an n-channel organic semiconductor
  16. AH10639 is a novel inhibitor of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase.
  17. Beclamide is a chlorinated benzylpropanamide used as an anticonvulsant drug. It is used in the treatment of tonic-clonic seizyres and has sedative properties.
  18. NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.
  19. 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).
  20. Nafocare B1 is a synthetic immune biological response modifier.
  21. NFTs tracer

    MK-6240 is a positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs), exhibiting high specificity and selectivity for binding to NFTs.
  22. PET tracer

    T807 a novel tau positron emission tomography (PET) tracer.
  23. TN1

    HbF inducer

    TN1 is a potent fetal hemoglobin (HbF) inducer.
  24. Dansyl glutathione is a trapping agent for the quantitative estimation and identification of reactive metabolites.
  25. IGPS inhibitor

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

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

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

    3-Methylpyrazole is used as a nitrification inhibitor of nitrification in soil.
  29. F 16915 is a docosahexaenoic acid derivative which can prevent heart failure-induced atrial fibrillation.
  30. 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.
  31. BAL-30072, a siderophore sulfactam, is a monocyclic beta-lactam antibiotic, with activity against multiresistant gram-negative bacilli.
  32. PCA-1/ALKBH3 inhibitor

    HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo.
  33. E-982 is extracted from the reference, compound 12.
  34. fibrinogen receptor antagonist

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

  35. memory-enhancing agent

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

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

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

    bronchodilator

    FKK is an indazole derivative and also a novel bronchodilator.
  43. 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.
  44. Cease inhibitor

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

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

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

    Voxelotor (GBT 440) is an orally bioavailable sickle hemoglobin (HbS) polymerization inhibitor.
  49. 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.
  50. Glufosfamide is a novel alkylating agent in which the active metabolite of isophosphoramide mustard is glycosidically linked to β-D-glucose.

Items 551-600 of 980

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