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  1. Azelaic acid is an organic compound produced by the ozonolysis of oleic acid; component of a number of hair and skin conditioners.
  2. Dehydrocholic acid is a synthetic bile acid, manufactured by the oxidation of cholic acid.
  3. RS-1 is a RAD51-stimulatory compound, which increases the DNA binding activity of RAD51.
  4. Sulisobenzone is an ingredient in some sunscreens which protects the skin from damage by UVB and short-wave UVA ultraviolet light.
  5. Glutathione acts as an antioxidant, a free radical scavenger and a detoxifying agent.
  6. L-tyrosine is a non-essential amino acid. In animals it is synthesized from Ephenylalanine.
  7. cell cycle inhibitor

    ON-013100 is a cell cycle inhibitor and is potentially useful for the treatment of mantle cell lymphoma.
  8. Fibrillogenesis inhibitor

    Eprodisate is an orally available disodium salt form of eprodisate, a negatively charged sulfonated inhibitor of fibrillogenesis, that can be used in the treatment of amyloid A (AA) amyloidosis.
  9. SCH00013 is a cardiotonic agent that primarily acts via an increase in myofibrillar Ca++ sensitivity, have a significant Ca(2+)sensitizing effect at pH 7.2 to 7.4.
  10. VMAT2 inhibitor

    Valbenazine is a potent and selective VMAT2 inhibitor.
  11. Cytohesin inhibitor

    SecinH3 is a selective cytohesin inhibitor with IC50 of 2.4 μM, 5.4 μM, 5.4 μM, 5.6 μM, 5.6 μM, and 65 μM for hCyh2, hCyh1, mCyh3, hCyh3, drosophila steppke, and yGea2-S7, respectively.
  12. 3,3'-Diindolylmethane(DIM) is a major digestive product of indole-3-carbinol, a potential anticancer component of cruciferous vegetables.
  13. HMN-176 is a stilbene derivative which inhibits mitosis without significant effect on tubulin polymerization.
  14. HTHQ, which is a hydroquinone monoalkyl ether, is a potent anti-oxidative agent, even at low dose levels.
  15. 2-Aminoheptane is a nasal decongestant drug which is a sympathomimetic stimulant and vasoconstrictor.
  16. 4-Aminohippuric acid is a typical substrate of organic anion transport systems.
  17. 6-Acetamidohexanoic acid is a pharmaceutical intermediate.
  18. Aceglutamide is a psychostimulant, nootropic agent which functions as a prodrug to glutamine with improved potency and stability.
  19. Acesulfame potassium is a non-nutritive sweetener.
  20. Acetylleucine is a drug used in the treatment of vertigo.
  21. Aminoguanidine is a diamine oxidase and nitric oxide synthase inhibitor. It acts to reduce levels of advanced glycation end products (AGEs) through interacting with 3-deoxyglucosone.
  22. Antimony potassium tartrate trihydrate is a powerful emetic, also used in the treatment of schistosomiasis and leishmaniasis.
  23. Azaguanine-8 is a purine analogs showing antineoplastic activity by competing with guanine in the metabolism.
  24. Carbazochrome sodium sulfonate (AC-17) is an antihemorrhagic for use in the treatment of hemorrhoids.
  25. Carbimazole is an imidazole antithyroid agent.
  26. Carzenide is an organic synthesis intermediate, used for synthetic drug.
  27. Chromocarb is a synthetic vasoprotectant.
  28. Cinchophen is an analgesic drug that is frequently used to treat gout.
  29. Citiolone is a derivative of the amino acid cysteine, used in liver therapy.
  30. Cysteamine is an agent for the treatment of nephropathic cystinosis and an antioxidant.
  31. Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA.
  32. hydroxyl radical-specific scavenger

    Nicaraven is a novel chemically synthesized hydroxyl radical-specific scavenger.
  33. 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.
  34. 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.
  35. 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.
  36. Type-I Kinase Inhibitor

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

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

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

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

    GR148672X is a TGH inhibitor.
  41. 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.
  42. ELN484228 is a cell-permeable alpha-Synuclein Blocker.
  43. 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.
  44. metal chelator

    Succimer is an orally active heavy metal chelator.
  45. Pirinixil is a hypolipidemic agent of low toxicity.
  46. Diflumidone is a non-steroidal antiinflammatory drug.
  47. Anitrazafen is a topically effective antiinflammatory agent.
  48. PME-1 inhibitor

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

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

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