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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC71136 | β-L-Fucopyranosyl phosphate |
β-L-Fucopyranosyl phosphate can be used for the research of carbohydrate metabolism. Glycosyl phosphates play crucial roles in carbohydrate metabolism as metabolic regulators or ubiquitous intermediates for glycoconjugate biosynthesis.
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| DC71135 | YZ9 |
Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 µM. Y29 also inhibits the HeLa cell growth with a GI50 of 2.7 µM.
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| DC71120 | Sulfo-GMBS |
Sulfo-GMBS is a cross-linker. Among the amine-sulfhydryl cross-linkers, Sulfo-GMBS generated the largest number of cross-links and covered most of the cross-links that were identified with AMAS and GMBS.
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| DC71119 | Suc-Gly-Pro-AMC |
Suc-Gly-Pro-AMC is a fibroblast activation protein (FAP)-specific substrate. Suc-Gly-Pro-AMC can be used to study the activity of FAP.
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| DC71117 | Sorbicillin |
Sorbicillin, a sorbicillinoid analogue, acts as a potent anti-inflammation agent.
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| DC71113 | Saponin PE |
Saponin PE is a saponin compound isolated from aerial part of Clematis tangutica.
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| DC71107 | Resolvin E2 |
Resolvin E2 ((-)-Resolvin E2), a proresolving lipid mediator, is useful as a lead for anti-inflammatory agent.
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| DC71105 | Pseudoisocyanine iodide |
Pseudoisocyanine (iodide) is a pan inhibitor of monoamine transporters and organic cation transporters with antidepressant-like activity.
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| DC71099 | Paroxetine |
Paroxetine, a phenylpiperidine derivative, is a potent and selective serotonin reuptake inhibitor (SSRI). Paroxetine is a very weak inhibitor of norepinephrine (NE) uptake but it is still more potent at this site than the other SSRIs.
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| DC71093 | Nonacosadiene |
Nonacosadiene is the pheromone of Drosophila melanogaster from a tetrahydrophyridine derivative.
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| DC71087 | MRS4620 |
MRS4620 is a potent CD73 inhibitor, with a Ki of 0.436 nM. MRS4620 can be use for the research of cancer immunotherapy.
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| DC71085 | MoTP |
MoTP is a specific platelet activating factor receptor antagonist and can induce melanocyte ablation. MoTP can be used for the research of cancer.
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| DC71083 | MitoTracker Green FM |
MitoTracker Green FM is a green-fluorescent dye that can selectively accumulate in the mitochondrial matrix. MitoTracker Green FM covalently binds to mitochondrial proteins by reacting with free thiol groups of cysteine residues.
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| DC71082 | MitoPerOx |
MitoPerOx is a fluorescent ratio-probe of lipid peroxidation. MitoPerOx can be taken up very rapidly into mitochondria within cells, thereby responding to changes in mitochondrial lipid peroxidation.
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| DC71080 | Maresin 2 |
Maresin 2 is an anti-inflammatory and pro-resolving mediator from human macrophages. Maresins are a new family of anti-inflammatory and pro-resolving lipid mediators biosynthesized from docosahexaenoic acid (DHA) by macrophages.
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| DC71078 | Makisterone A |
Makisterone A, a 28-carbon moulting hormone, has been identified as the major free pupal ecdysteroid in the honey bee, Apis mellifera.
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| DC71074 | Loliolid |
Loliolide, a Carotenoid Metabolite, is a potential endogenous inducer of herbivore resistance. Loliolide also inhibits the seedling growth.
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| DC71073 | Linoleyl methane sulfonate |
Linoleyl methane sulfonate is a selective lipid-based vehicle for use in drug delivery systems.
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| DC71072 | Levatin |
Levatin is an 18-Norclerodane diterpene from Croton levatii.
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| DC71065 | Jineol |
Jineol is a cytotoxic alkaloid from the centipede Scolopendra subspinipes. Jineol exhibits modest cytotoxic activity in vitro against the growth of human tumor cell lines.
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| DC71058 | Inositol nicotinate |
Inositol nicotinate, with vasodilatory effect, is used in the study of Peripheral arterial disease (PAD).
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| DC71053 | H-Glu(Met-OH)-OH |
H-Glu(Met-OH)-OH could induce oxidation of hydroxyl radical.
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| DC71051 | Green CMFDA |
Green CMFDA (CMFDA) is a cell-permeable fluorescent probe that can be used a cell tracer. Green CMFDA can be cleaved by non-specific esterases common to living cells, producing a fluorescent compound, fluorescein, visible using a fluorescent microscope.
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| DC71050 | GP3269 |
GP3269 is a potent, selective, and orally active inhibitor of human adenosine kinase (AK) with an IC50 of 11 nM. GP3269 exhibits anticonvulsant activity in rats.
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| DC71048 | Glycolithocholic acid sodium |
Glycolithocholic acid sodium is the sodium salt of Glycolithocholic acid. Glycolithocholic acid is a glycine-conjugated secondary bile acid. Glycolithocholic acid can be used to diagnose ulcerative colitis (UC), non-alcoholic steatohepatitis (NASH) and primary sclerosing cholangitis (PSC).
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| DC71043 | Flocoumafen |
Flocoumafen (WL 108366), a second-generation anticoagulant rodenticide (ARs), belongs to the family of vitamin K antagonist (VKA) molecules.
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| DC71041 | Fenadiazole |
Fenadiazole acts as a central nervous system agent to manage insomnia and dreaminess.
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| DC71037 | EUK-118 |
EUK-118 is an analog of EUK 8 and EUK 134 with reduced activity. EUK-118 exhibits superoxide dismutase (SOD) mimetic activity.
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| DC71035 | Emylcamate |
Emylcamate is a potent muscle relaxant. Emylcamate has the potential for the research of neurological diseases.
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| DC71031 | Deschloro Cetirizine dihydrochloride |
Deschloro Cetirizine Dihydrochloride is a Cetirizine impurity. Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist.
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