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Cat. No. Product Name Field of Application Chemical Structure
DC65933 WAY-622216 Featured altering the lifespan of a eukaryotic organism; anti-viral;
DC65934 2-(Thiobenzoylthio)propionic acid Featured
DC65935 Enterobactin Featured Enterobactin is a high affinity siderophore that acquires iron for microbial systems.
DC65936 (S)-BnCH2-PyBox, (S,S)-2,6-Bis(4-benzylmethyl-2-oxazolin-2-yl)pyridine Featured
DC65937 clenpirin Featured Clenpirin is a bio-active chemical.
DC65938 Naphthol AS-TR Phosphate Disodium Salt Featured Naphthol AS-TR Phosphate disodium is a water-soluble dye commonly used as an enzymatic substrate in various biochemical assays to detect alkaline phosphatase activity. Naphthol AS-TR Phosphate disodium has unique chemical properties that allow it to be hydrolyzed by alkaline phosphatase, forming a colored product that can be detected spectrophotometrically. This makes it a useful tool for monitoring enzyme activity in biological samples such as serum or urine.
DC65939 [bromo(difluoro)methyl]benzene Featured
DC65940 3-((1-carboxyvinyl)oxy)benzoic acid Featured
DC65941 AF615 Featured
DC65942 4-Ethynyl-N-ethyl-1,8-napthalamide Featured
DC65943 Naphthol AS-BI phosphate disodium salt Featured
DC65944 N406211 Featured
DC65945 Imiloxan hydrochloride Featured Imiloxan hydrochloride is a potent and selective alpha 2B-adrenoceptor antagonist. Imiloxan hydrochloride has the potential for acute kidney injury research.
DC65946 (R)-(-)-α-Methylhistamine dihydrobromide Featured (R)-(-)-α-Methylhistamine dihydrobromide is a potent, selective and brain-penetrant agonist of H3 histamine receptor, with a Kd of 50.3 nM. (R)-(-)-α-Methylhistamine dihydrobromide can enhance memory retention, attenuates memory impairment in rats.
DC65947 (S)-(+)-2-Chlorophenylglycine Methyl Ester Tartrate Salt Featured
DC65948 2-Chloromethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine, Hydrochloride Featured
DC65949 2-Mercaptobenzimidazole Featured
DC65950 (S)-(+)-2-Chlorophenylglycine Methyl Ester Featured
DC65951 PTP1B-IN-4 Featured PTP1B-IN-4 is a non-competitive allosteric inhibitor of the protein tyrosine phosphatase PTP1B, with an IC50 of 8 μM. PTP1B-IN-4 is potentail for the research of obesity and diabetes.
DC65952 10-Hydroxygeraniol Featured
DC65953 10-Formyl Folic Acid Featured 10-Formylfolic acid is a potent inhibitor of dihydrofolate reductase.
DC65954 OTUB1/USP8 inhibitor 61 Featured OTUB1/USP8-IN-1 is a potent dual OTUB1/USP8 inhibitor with IC50 values of 0.17 and 0.28 nM for OTUB1 and USP8, respectively. OTUB1/USP8-IN-1 can be used in research of cancer.
DC65955 GOSLO SR 5-69 Featured GoSlo-SR-5-69 is a potent activator of large conductance Ca2+-activated K+ (BK) channels, with an EC50 of 251 nM.
DC65956 Dicyclopenta[b,e]pyridin-8(1H)-imine, 2,3,4,5,6,7-hexahydro-4-methyl- Featured
DC65957 8-Azabicyclo[3.2.1]octane-8-carboxamide, 3-(2-pyridinylsulfonyl)-N-[4-(trifluoromethyl)phenyl]- Featured
DC65958 3-Hydroxy-4,5-bis-benzyloxy-6-benzyloxymethyl-2-phenyl2-oxo-2λ5-[1,2]oxaphosphinane Featured
DC65959 Vocacapsaicin hydrochloride Featured Use of Vocacapsaicin hydrochloride Vocacapsaicin (CA-008) hydrochloride, a prodrug of Capsaicin, is a first-in-class non-opioid TRPV1 agonist. Vocacapsaicin hydrochloride can provide meaningful and long-lasting pain relief.
DC72935 JSF-2414 Featured JSF-2414 (JSF2414) is a potent, small molecule GyrB/ParE dual binding inhibitor, simultaneously binds to ATP binding regions of DNA gyrase (GyrB) and topoisomerase (ParE) and displays potent in vitro activity against strains of MRSA, VRSA and VISA.
DC72952 Savirin Featured Savirin (S. aureus virulence inhibitor) is a small molecule that targets the agr (accessory gene regulator) quorum sensing system in Staphylococcus aureus (S. aureus). The agr system is a key regulatory pathway that controls the expression of virulence factors in S. aureus, which are critical for its pathogenicity. The system involves a two-component signal transduction pathway consisting of AgrC (a histidine kinase) and AgrA (a response regulator).
DC72970 Cotransin CT8 Featured Cotransin CT8 (CT-08) is a substrate-selective co-translational translocation inhibitor, binds the Sec61 translocon to inhibit cotranslational translocation of a subset of secreted and type I transmembrane proteins.

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