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Guanosine 5'-triphosphate trisodium salt
Catalog No. A18283 Guanosine 5'-triphosphate trisodium salt (5'-GTP trisodium salt) is an activator of signal transduction of G proteins. 了解更多 -
6-Diazo-5-oxo-L-nor-Leucine
Catalog No. A20846 6-Diazo-5-oxo-L-norleucine 是一种从链霉菌中分离出来的抗生素，一种 glutaminase 的拮抗剂对cKGA（肾脏型谷氨酰胺酶）的IC50值约为1 mM。 了解更多 -
Docosahexaenoic Acid
Catalog No. A18205 Docosahexaenoic Acid (DHA) is an omega-3 fatty acid abundantly present brain and retina. It can be obtained directly from fish oil and maternal milk. 了解更多 -
Corticosterone
Catalog No. A14269 Corticosterone 是一种具有口服活性的，由肾上腺皮质产生的糖皮质激素，在调节边缘系统 (包括海马体、前额叶皮层和杏仁核) 的神经元功能方面起着重要作用。皮质酮可通过 SGK 诱导的 GDI 磷酸化增加 Rab 介导的 AMPAR 膜运输. 了解更多 -
Triphala
Catalog No. A16067 Anti-adipogenic, anti-inflammatory, and anti-neoplastic activitiesTriphala, an Ayurvedic polyherbal formulation comprising of equiproportional fruit parts of Terminalia chebula, Terminalia bellerica, and Phyllanthus emblica. Triphala inhibits NF-κB activation. Triphala exerts antifungal action. Anti-adipogenic, anti-inflammatory, and anti-neoplastic activities. 了解更多 -
Adenosine deaminase
Catalog No. A19330 Adenosine deaminase is an enzyme that catalyzes the irreversible deamination of adenosine and 2'-deoxyadenosine to inosine and 2'-deoxyinosine, respectively. 了解更多 -
Angiotensin III
Catalog No. A18943 angiotensin 1 (AT1) and AT2 receptor agonistAngiotensin III is an angiotensin 1 (AT1) and AT2 receptor agonist. 了解更多 -
Pertussis Toxin
Catalog No. A19356 protein-based AB5-type exotoxinPertussis Toxin is a protein-based AB5-type exotoxin produced by the bacterium Bordetella pertussis, which causes whooping cough. 了解更多 -
Calf thymus DNA
Catalog No. A20155 Calf thymus DNA (DNA from calf thymus) is high quality double-stranded template DNA isolated from the thymus of male and female calves. 了解更多 -
Chitosan oligosaccharide
Catalog No. A20304 Chitosan oligosaccharide (COS) is an oligomer of β-(1??4)-linked D-glucosamine. Chitosan oligosaccharide (COS) activates AMPK and inhibits inflammatory signaling pathways including NF-κB and MAPK pathways. 了解更多 -
Hypotaurine
Catalog No. A20590 Hypotaurine (2-aminoethanesulfinic acid), an intermediate in taurine biosynthesis from cysteine in astrocytes, is an endogenous inhibitory amino acid of the glycine receptor. 了解更多 -
Calcium polystyrene sulfonate
Catalog No. A18233 used to treat hyperkalemia in patients with chronic kidney disease (CKD)Calcium polystyrene sulfonate is an ion-exchange resin used for reducing blood levels of potassium. Calcium polystyrene sulfonate is used to treat hyperkalemia in patients with chronic kidney disease (CKD). 了解更多 -
Hyaluronidase
Catalog No. A18232 local anesthetic additiveHyaluronidase (Hyaluronate 4-glycanohydrolase; Hyaluronoglucosaminidase) is a naturally occurring enzyme that depolymerizes hyaluronic acid by cleavage of glycosidic bonds and has been used as a local anesthetic additive. 了解更多 -
Cinnamylamine
Catalog No. A20835 Cinnamylamine can be used for the preparation of Tranylcypromine, a drug that acts as a nonselective and irreversible inhibitor of the enzyme monoamine oxidase (MAO), and is used as an antidepressant and anxiolytic agent. 了解更多 -
Peptide 401
Catalog No. A13913 Peptide 401, a potent mast cell degranulating factor from bee venom, suppresses the increased vascular permeability due to intradermal injection of various smooth muscle spasmogens (histamine, and 5-HT). 了解更多 -
Apilimod mesylate
Catalog No. A22049 IL-12/IL-23 inhibitorApilimod (STA 5326) mesylate is a potent IL-12/IL-23 inhibitor, and strongly inhibits IL-12 with IC50s of 1 nM and 2 nM, in IFN-γ/SAC-stimulated human PBMCs and SAC-treated monkey PBMCs, respectively. 了解更多 -
LC3-mHTT-IN-AN1
Catalog No. A22054 mHTT-LC3 linker compoundLC3-mHTT-IN-AN1 (Compound AN1) is a mHTT-LC3 linker compound, which interacts with both mutant huntingtin protein (mHTT) and LC3B but not with wtHTT or irrelevant control proteins. 了解更多 -
APX-115 free base
Catalog No. A22055 pan NADPH oxidase (Nox) inhibitorAPX-115 free base (Ewha-18278 free base) is a potent, orally active pan NADPH oxidase (Nox) inhibitor with Ki values of 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2 and Nox4, respectively. 了解更多 -
Mizagliflozin
Catalog No. A22056 SGLT1 inhibitorMizagliflozin (DSP-3235 free base) is a potent, orally active and selective SGLT1 inhibitor, with a Ki of 27 nM for human SGLT1. 了解更多 -
TLR4-IN-C34
Catalog No. A22057 TLR4 inhibitorTLR4-IN-C34 is an orally active TLR4 inhibitor and reduces systemic inflammation in models of endotoxemia and necrotizing enterocolitis. 了解更多 -
DIMBOA
Catalog No. A22058 -
H-β-Ala-AMC TFA
Catalog No. A22059 -
PF-04745637
Catalog No. A22060 -
Filastatin
Catalog No. A22063 Candida albicans filamentation inhibitorFilastatin is a long-lasting inhibitor of Candida albicans filamentation. Filastatin inhibits adhesion by multiple pathogenic Candida species with an IC50 of ~3 μM in the GFP-based adhesion assay. 了解更多 -
Neuraminidase-IN-1
Catalog No. A22065 neuraminidase inhibitorNeuraminidase-IN-1 is a neuraminidase inhibitor, with an IC50 of 0.21 μM. Neuraminidase-IN-1 has excellent activity against H1N1 influenza virus. 了解更多 -
BAY 2416964
Catalog No. A22067 aryl hydrocarbon receptor (AHR) antagonistBAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist extracted from patent WO2018146010A1, example 192, has an IC50 of 341 nM. BAY 2416964 has the potential for solid tumors treatment. 了解更多
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