Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN484221 Meseclazone 29053-27-8
Meseclazone (W2395;NSC297623) exhibits inhibitory potency of secondary phase ADP aggregation. Meseclazone possesses anti-inflammatory, analgesic and antipyretic activity.
YN330648 7,3',4'-Tri-O-methylluteolin 29080-58-8
7,3',4'-Tri-O-methylluteolin (5-Hydroxy-3',4',7-trimethoxyflavone) is a flavonoid from the herbLippia nodifloraL. (Verbenaceae) which has been documented to exhibit anti-inflammatory, antipyretic, antitussive, antidiabetic, anticancer...
YN480307 Procyanidol B4 29106-51-2
Procyanidol B4 ((-)-Procyanidin B4) is a flavanol, isolated fromLitchi chinensis. Anti-inflammatory properties.
YN321695 Mequitazine 29216-28-2
Mequitazine is a histamine H1 antagonist which competes with histamine for the normal H1-receptor sites on effector cells of the gastrointestinal tract, blood vessels and respiratory tract.
YN482775 Genipin 1-β-D-gentiobioside 29307-60-6
Genipin 1-β-D-gentiobioside (Genipin 1-gentiobioside) is one of the most abundant and bioactive iridoid glycosides inGardenia jasminoidesEllis, which possesses hepatoprotective, anti-inflammatory, antioxidant, and antithrombotic a...
YN482669 Tabersonine hydrochloride 29479-00-3
Tabersonine, an ingredient extracted from the bean of Voacanga africana, is a potent inhibitor against Aβ(1?42) aggregation and toxicity.
Negletein is a neuroprotectant enhances the action of nerve growth factor and induces neurite outgrowth in PC12 cells. Negletein shows promising anti-inflammatory activity via inhibition ofTNF-α and IL-1βwith IC50 values of 1...
Astilbin, a flavonoid compound isolated from the rhizome of Smilax glabra Roxb, displays anticancer, antioxidative, anti-inflammatory, and immunosuppressive activities.
YN321107 Pirenzepine dihydrochloride 29868-97-1
Pirenzepine is an antimuscarinic agent which inhibits gastric acid secretion at lower doses than are required to affect gastrointestinal motility, salivary, central nervous system, cardiovascular, ocular and urinary functions.
YN481355 Nicotredole 29876-14-0
Nicotredole (Tryptamide) is an orally active anti-inflammatory and analgesic agent. Nicotredole exhibits evident antiinflammatory effects of potency comparable with Phenylbutazone. Nicotredole has only weak ulcerogenic activity .
YN372833 S-Adenosyl-L-methionine 29908-03-0
Ademetionine, also known as SAMe, is a specific form of the amino acid methionine known as S-adenosyl-methionine. It is essential for the formation of glutathione, a water-soluble peptide that helps the body fight free radicals.
Licraside is isolated fromGlycyrrhiza uralesis Fish.
PPA-904 is a specific phenothiazinephotosensitizerin photodynamic therapy (PDT) research, especially topical application for cutaneous leishmaniasis in vivo.
YN322026 Oxitropium Bromide 30286-75-0
Oxitropium bromide is anmAChRantagonist used as an anticholinergic bronchodilator drug for the treatment of asthma and chronic obstructive pulmonary disease.
SDMA (Symmetric dimethylarginine) is an endogenous inhibitor of nitric oxide (NO) synthase activity.
YN350262 Pseudocoptisine acetate 30426-66-5
Pseudocoptisine acetate, a quaternary alkaloid with a benzylisoquinoline skeleton, is isolated from the tubers ofCorydalis turtschaninovii. Pseudocoptisine acetate shows anti-inflammatory properties.
YN373318 Licoricidin 30508-27-1
Licoricidin (LCD) is isolated fromGlycyrrhiza uralensis Fisch, possesses anti-cancer activities. Licoricidin (LCD) inhibit SW480 cells (IC50=7.2μM) by inducing cycle arrest,apoptosis and autophagy, and is a potential chemo...
YN330340 Etofenamate 30544-47-9
Etofenamate is a nonsteroidal anti-inflammatory drug (NSAID) used for the treatment of joint and muscular pain.
YN350257 Bisabolangelone 30557-81-4
Bisabolangelone, a sesquiterpene derivative, is isolated from the roots of Osterici Radix. Bisabolangelone possesses anti-inflammatory properties, which inhibits LPS-stimulated inflammation through the blocking ofNF-kappaB and MA...
YN372271 Geldanamycin 30562-34-6
Geldanamycin is a natural existing HSP90 inhibitor with Kd of 1.2 μM, specifically disrupts glucocorticoid receptor (GR)/HSP association.
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