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  1. N-Bis(2-hydroxypropyl)nitrosamine is an agent with carcinogenic activity.
  2. 7-Methyluric Acid is a metabolite of Theobromine.
  3. 3-Methylcrotonyl Glycine is a metabolite found in 3-methylcrotonylglycinuria, a metabolic disorder.
  4. Hexanoyl glycine is an acylated amino acid that is used as a urinary biomarker for several indications.
  5. 6-Maleimido-1-hexanol is a maleimide compound with a pendant hexanol moiety.
  6. Biotinyl Cystamine is a crosslinking photoaffinity label ligand.
  7. cis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
  8. a-Hydroxyglutaric acid (2-HG) is an a-hydroxy acid. It is normally metabolized to 2-oxoglutarate by D- and L-2-hydroxyglutarate dehydrogenases, and mutations in these enzymes cause 2-hydroxyglutaric aciduria, a neurometabolic disorder.
  9. Etofenamate is an anti-inflammatory, anti-arrhythmic amino acid.
  10. Anticancer agent 3 (Compound 4) is a anti-cancer agent.
  11. Nifuratel is used as an antibacterial, antifungal, and antiprotozoal (Trichomonas).
  12. Phloroglucinol is a hygroscopic biochemical that is also potentially useful for bone decalcification in microscopy specimens or the detection of wood fibers.
  13. Gefarnate is a synthetic isoprenoid that is used to treat chronic gastric and duodenic ulcers.
  14. Levomefolic acid is the primary biologically active form of folic acid used at the cellular level for DNA reproduction, the cysteine cycle and the regulation of homocysteine.
  15. N-cadherin antagonist

    Exherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities.
  16. PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothiazin-10-yl)propane-1-sulfonate.
  17. Gemcitabine elaidate is a lipophilic, unsaturated fatty acid ester derivative of gemcitabine (dFdC), an antimetabolite deoxynucleoside analogue, with potential antineoplastic activity.
  18. ENT1 inhibitor

    NBMPR is a nucleoside analog that competitively inhibits the equilibrative nucleoside transporter 1 (Kd = 0.1-1.0 nM, IC50s = 4.6 and 3.6 nM in rat and human, respectively).
  19. Treprostinil is a stable analog of prostacyclin that is used clinically for the treatment of PPH.
  20. NSI-189 is a nootropic and neurogenic research chemical derived from nicotinamide and pyrazine.
  21. GDP exchange inhibitor

    SCH 54292 is a novel GDP exchange inhibitor
  22. rRNA modificator

    5S rRNA modificator is a suitable electrophile for 2?€?-hydroxyl acylation on structured RNA molecules, yielding accurate structural information comparable to that obtained with existing probes; 5S rRNA RNA modification.
  23. Cambendazole acts as an anthelmintic used in the treatment of Chagas?€? disease.
  24. ST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
  25. AdipoR1 and AdipoR2 agonist

    AdipoRon is a novel small-molecule AdipoR agonist; binds to both AdipoR1(Kd= 1.8 uM) and AdipoR2(Kd=3.1 uM). IC50 value: 1.8/3.1 uM(AdipoR1/2, Kd)
  26. Ononetin is a naturally occurring deoxybenzoin.
  27. GPIIb/IIIa antagonist

    Tirofiban, Hydrochloride Hydrate is a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist.
  28. Bioluminescent substrate

    D-Luciferin is a popular bioluminescent substrate of luciferase in the presence of ATP, used in luciferase-based bioluminescence imaging and cell-based high-throughput screening applications.
  29. Clodronate disodium is the disodium salt of a nitrogen-free bisphosphonate analog of naturally occurring pyrophosphate.
  30. leukemia inhibitory factor (LIF) inhibitor

    EC330 is a leukemia inhibitory factor (LIF) inhibitor.
  31. Atopaxar hydrobromide shows potent inhibitory effects on human platelet aggregation induced by thrombin and TRAP with IC values of 0.064 and 0.031 μM respectively.
  32. Photochlor is a lipophilic, second-generation, chlorin-based photosensitizer. Upon intravenous administration, HPPH selectively accumulates in the cytoplasm of cancer or pre-cancerous cells.
  33. (S)-Reticuline is the (S)-enantiomer of Reticuline. An enantiomer of a tetrahydrobenzylisoquinoline alkaloid. Reticuline is a chemical compound found in a variety of plants including Lindera aggregata, Annona squamosa, and Ocotea fasciculata.
  34. DCPS inhibitor

    RG3039 (PF-06687859) is orally bioavailable, brain-penetrant small molecule that has been shown to be an inhibitor of the mRNA decapping enzyme, DcpS.
  35. AC 42 is an allosteric agonist.
  36. morpholino antisense oligomer

    Eteplirsen is an experimental drug, currently in clinical trials.
  37. METAP2 inhibitor

    Beloranib, an analog of the natural chemical compound fumagillin, is an inhibitor of the enzyme METAP2.
  38. TP-434 is a novel, broad-spectrum fluorocycline antibiotic with activity against bacteria expressing major antibiotic resistance mechanisms including tetracycline-specific efflux and ribosomal-protection.
  39. Desmethyldoxepin is the primary metabolite of doxepin, produced by metabolism at the liver. Doxepin is a tricyclic antidepressant.
  40. Noscapine is an orally administrable drug used worldwide for cough suppression, primarily mediated by its sigma receptor agonist activity, and possess anticancer activity.
  41. sympathetic ganglioblocker

    Fluorocurarine chloride is a short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction.
  42. SM-130686 is a potent, orally active growth hormone secretagogue, with around half the potency of the endogenous agonist ghrelin as a stimulator of growth hormone release.
  43. TPT-260 is a thiophene thiourea derivative.
  44. PR-104 is a non-toxic, small-molecule, hypoxia-activated, 3,5-dinitrobenzamide nitrogen mustard pre-prodrug with potential antitumor activity.
  45. Fosfluconazole is a water-soluble phosphate prodrug of fluconazole - a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.
  46. K-252a is a metabolite originally isolated from the culture broth of Nocardiopsis sp.. Experiments have shown that at high concentrations this compound is an ATP-competitive inhibitor of cyclic nucleotide-dependent protein kinases.
  47. MetAP-2 inhibitor

    TNP 470 is an analog of Fumagillin that displays potent antiangiogenic activity in vitro. Shown to inhibit MetAP-2 (methionine aminopeptidase type II ).
  48. Alpha-galactosidase inhibitor

    Deoxygalactonojirimycin Hydrochloride is a potent and selective Alpha-gal A (Alpha-galactosidase) inhibitor.
  49. Chlorin E6 is a natural molecule and a promising photosensitizer.
  50. Biotin hydrazide is a biotinyl derivative that can be used as a probe for the determination of protein carbonylation, which is a component of several diseases.

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