Catalog No.
Product Name
Application
Product Information
Citations
- Dimethyl 4-hydroxyisophthalate is a methyl salicylate analogue.
- 3-arylisoquinolinamine derivative is a 3-arylisoquinolinamine derivative with antitumor activity.
- Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity.
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Noradrenalin re-uptake inhibitor
Nisoxetine hydrochloride is a selective and potent inhibitor of norepinephrine transporter with little or no affinity for a range of other neurotransmitter receptors. Nisoxetine hydrochloride is an inhibitor of SLC6A2. -
GSK369796 Dihydrochloride Shows antimalerial activity with IC50 values of 11.2 nM for 3D7 strain, 12.6 nM for HB3 strain, 17.6 nM for K1 strain
- Golotimod is an orally bioavailable synthetic peptide containing the amino acids D-glutamine and L-tryptophan connected by a gamma-glutamyl linkage with potential immunostimulating, antimicrobial and antineoplastic activities.
- BMS-747158-02 is a fluorine 18?Clabeled pyridaben derivative designed as a new myocardial perfusion imaging agent for use with positron emission tomography (PET).
- N-Methyl Metribuzin is an aminotriazinone and the methylamine analogue of the herbicide Metribuzin.
- Metazathioprine is a methylated derivative of azathioprine (AZA). It demonstrated the greatest values of apparent and specific partition coefficients in n-octanol/phosphate buffer at pH 5.7 and pH 7.4 among purine derivatives such as 6-mercaptopurine (6-MP), 6-thioguanine (6-TG) and AZA.
- Isatoribine monohydrate is a novel guanosine analogue showing immunostimulatory activity both in vivo and in vitro. This compound acts on different components of the immune system including B cells, natural killer (NK) cells and antigen-presenting cells (APC).
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PKR Inhibitor
PKR Inhibitor is an oxindole/imidazole derivative that binds the ATP-binding site of PKR and blocks autophosphorylation with an IC50 value of 186-210 nM.3 PKR Inhibitor protects human neuroblastoma cells against cell damage triggered by tunicamycin-mediated endoplasmic reticulum stress. - N-(p-Coumaroyl) Serotonin is an antibacterial agent which inhibits the production of proinflammatory cytokines by LPS-stimulated human blood monocytes.
- N-Bis(2-hydroxypropyl)nitrosamine is an agent with carcinogenic activity.
- 3-Methylcrotonyl Glycine is a metabolite found in 3-methylcrotonylglycinuria, a metabolic disorder.
- 6-Maleimido-1-hexanol is a maleimide compound with a pendant hexanol moiety.
- cis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
- 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.
- Phloroglucinol is a hygroscopic biochemical that is also potentially useful for bone decalcification in microscopy specimens or the detection of wood fibers.
- 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.
- Gemcitabine elaidate is a lipophilic, unsaturated fatty acid ester derivative of gemcitabine (dFdC), an antimetabolite deoxynucleoside analogue, with potential antineoplastic activity.
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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). -
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. - Cambendazole acts as an anthelmintic used in the treatment of Chagas?€? disease.
- ST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
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GPIIb/IIIa antagonist
Tirofiban, Hydrochloride Hydrate is a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist.

