Other inhibitors

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  1. Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA.
  2. hydroxyl radical-specific scavenger

    Nicaraven is a novel chemically synthesized hydroxyl radical-specific scavenger.
  3. Stemness kinase inhibitor

    Amcasertib (BBI503), a first-in-class cancer stemness kinase inhibitor, is claimed to inhibit Nanog and other CSC pathways by targeting kinases with potential anticancer activity.
  4. meta-Topolin is an aromatic cytokinin, first isolated from leaves of Populus x robusta. Cytokinins (CTKs) are a class of growth-regulating hormones involved in various physiological and developmental processes.
  5. Rio2 kinase (RIOK2) inhibitor

    NSC139021 (ERGi-USU) is a highly selective inhibitor for the growth of ERG-positive cancer cells with IC50s ranging from 30 to 400 nM.
  6. Type-I Kinase Inhibitor

    VI-16832 is a broad spectrum type-I kinase inhibitor
  7. LOXL2 inhibitor

    LOXL2-IN-1 HCl is a selective LOXL2 inhibitor with an IC50 of 126 nM.
  8. Analgesic

    Nifenazone is a drug used as an analgesic for a number of rheumatic conditions.
  9. antirheumatic drug

    Esonarimod is an antirheumatic drug, suppressing lymphocyte activating factor activity or biosynthesis.
  10. TGH inhibitor

    GR148672X is a TGH inhibitor.
  11. RPA inhibitor

    HAMNO, also known as NSC-111847, is a potent and selective inhibitor of replication protein A (RPA) interactions with proteins involved in the replication stress response.
  12. ELN484228 is a cell-permeable alpha-Synuclein Blocker.
  13. CPHPC is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. Serum amyloid P (SAP) is pentraxin with roles in inflammation and immune response.
  14. metal chelator

    Succimer is an orally active heavy metal chelator.
  15. Pirinixil is a hypolipidemic agent of low toxicity.
  16. Diflumidone is a non-steroidal antiinflammatory drug.
  17. Anitrazafen is a topically effective antiinflammatory agent.
  18. PME-1 inhibitor

    AMZ30 is a selective, covalent inhibitors of protein phosphatase methylesterase-1(PME-1) with IC50 value of 600 nM.
  19. GJ-103 is an active analog of the read-through compound GJ072. CAS: 1459687-96-7 (Sodium salt) 1459687-89-8 (Free Acid)
  20. NRP1 antagonist

    EG01377 TFA salt is a selective neuropilin-1 (NRP1) antagonist. CAS: 2227996-00-9 (Free base)
  21. MPI inhibitor

    MLS0315771 is a potent competitive phosphomannose isomerase (MPI) inhibitor.
  22. Sulfabromomethazine, also known as Bromosulfamethazine, NSC 5874, SN 3517, is a long-acting derivative of sulfamezathine that is used in the poultry, swine and cattle industries for the treatment of coccidiosis.
  23. ABHD16A inhibitor

    KC01 is a covalent inhibitor of ABHD16A.
  24. Chlorthalidone is a diuretic drug used to treat hypertension. It is described as a thiazide diuretic. Compared with other medications of the thiazide class, chlortalidone has the longest duration of action but a similar diuretic effect at maximal therapeutic doses. Chlortalidone is often used in the management of hypertension and edema. Chlorthalidone directly inhibits sodium and chloride reabsorption on the luminal membrane of the early segment in the distal convoluted tubule in the kidney. This leads to an increase in sodium, chloride, bicarbonate, and potassium secretion resulting in the excretion of water.
  25. Felbinac is a potent non-steroidal anti-inflammatory agent, used to treat muscle inflammation and arthritis.
  26. Phenethyl alcohol, or 2-phenylethanol, is the organic compound that consists of a phenethyl group group attached to OH. It is a colourless liquid that is slightly soluble in water, but miscible with most organic solvents.
  27. Carbasalate Calcium, also known as Alcacyl and Omegin, is a non-steroidal anti-inflammatory drug used to treat pain and fever.
  28. Metaxalone is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions. It is considered to be a moderately strong muscle relaxant, with relatively low incidence of side effects. Metaxalone appears to interact with the cytochrome p450 system and may act as a general central nervous system depressant.
  29. Oxaceprol is an antirheumatic Agent.
  30. Anisindione (brand name Miradon) is a synthetic anticoagulant and an indanedione derivative. It prevents the formation of active procoagulation factors II, VII, IX, and X, as well as the anticoagulant proteins C and S, in the liver by inhibiting the vitamin K?Cmediated gamma-carboxylation of precursor proteins.
  31. Suxibuzone is a analgesic used for joint and muscular pain. It is a prodrug of the non-steroidal anti-inflammatory drug phenylbutazone, and is commonly used in horses.
  32. Bendroflumethiazide is a thiazide diuretic used to treat hypertension. Bendroflumethiazide works by inhibiting sodium reabsorption at the beginning of the distal convoluted tubule and may play an important role in the treatment of mild heart failure.
  33. alpha-Tocopherol is one of the most abundant isoforms of vitamin E. alpha-Tocopherol is a biologically active liposoluble vitamin and potent antioxidant.
  34. skin permeation of drug

    Laurocapram is a chemical enhancer for skin permeation of drug.
  35. prodrug of paracetamol (PCM)

    Propacetamol Hydrochloride is a prodrug of paracetamol (PCM), being effectively used to treat fever and pain.
  36. vasodilator

    Xanthinol niacinate is a combination of xanthinol and niacin which acts as a vasodilator.
  37. Menbutone is an oxobutyric acid derivative and acts as a choleretic.
  38. central nervous system stimulant

    Nikethamide is a central nervous system stimulant. It is a clear light yellow viscous liquid or crystalline solid and has a slightly bitter taste followed by a faint sensation of the warmth.
  39. Antiarthritic

    Actarit is a drug that has been shown to suppress disease activity of rheumatoid arthritis (RA). Actarit reduces spontaneous tumor necrosis factor-alpha and interleukin 1beta secretion by primary synovial cells of patients with RA.
  40. non-steroidal anti-inflammatory

    Clonixin, also known as lysine clonixinate and Deltar, is a non-steroidal anti-inflammatory used in the treatment of migraines.
  41. Xipamide is a sulfamoylbenzamide analog of Clopamide. It is a diuretic as well as a saluretic with antihypertensive activity. It is bound to plasma proteins, thus has a delayed onset and prolonged action.
  42. antioxidant

    Sulbutiamine is an antioxidant that act by inhibiting oxidative stress induced retinal ganglion cell death.
  43. Iodixanol is a contrast agent. It is commonly used as a contrast agent during coronary angiography. It is the only iso-osmolar contrast agent, with an osmolality of 290 mOsm/kg H2O??the same as blood.
  44. Ufenamate is a topical analgesic.
  45. CPS1 activator

    Carglumic acid (N-Carbamyl-L-glutamic acid), a functional analogue of N-acetylglutamate (NAG) and a carbamoyl phosphate synthetase 1 (CPS1) activator, is used to treat acute and chronic hyperammonemia associated with NAG synthase (NAGS) deficiency.
  46. Bromisoval, also known as bromovalerylurea, is a bromide-containing sedative-hypnotic that is occasionally combined with non-steroidal anti-inflammatory drugs in over-the-counter products.
  47. anti-inflammatory

    Diflorasone is used in topical corticosteroids for its anti-inflammatory effect.
  48. Desoximetasone is a medication belonging to the family of medications known as topical corticosteroids. It is used for the relief of various skin conditions, including rashes. It helps to reduce redness, itching, and irritation.
  49. hyopglycemic agent

    Acetohexamide is a sulfonylurea derivative. Acetohexamide is a hyopglycemic agent with moderate uricosuric activity. Acetohexamide is a first generation medication used in the treatment of diabetes metilus type 2.
  50. anticonvulsant

    Phensuximide is an anticonvulsant in the succinimide class. It suppresses the paroxysmal three cycle per second spike and wave EEG pattern associated with lapses of consciousness in petit mal seizures. The frequency of attacks is reduced by depression of nerve transmission in the motor cortex.

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