Chemical structure
Cat.No.
Product Name
CAS no.
Target
NS-398 is a selective inhibitor of cyclooxygenase-2 (COX-2). The IC50 values for human recombinant COX-1 and -2 are 75 and 1.77 μM, respectively.
YN330337 Iguratimod 123663-49-0
Iguratimod is a small molecule compound with anti-inflammatory and immunomodulatory actions and used for the treatment of rheumatoid arthritis.
YN373565 Acetyl-Calpastatin(184-210)(... 123714-50-1
Acetyl-Calpastatin(184-210)(human) is a potent, selective and reversiblecalpaininhibitor with Ki values of 0.2nM and 6μM for µ-calpain and cathepsin L, respectively.
GR79236 is a highly potent, selective and orally activeadenosine A1 receptoragonist with aKis of 3.1nM and 1300nM forA1 and A2 receptors, respectively. GR79236 has anti-nociceptive and anti-inflammatory actions.
YN483080 6"-O-Malonyldaidzin 124590-31-4
6"-O-Malonyldaidzin is a malonylated isoflavone isolated from soybean seeds. 6"-O-Malonyldaidzin may has protective effect on eye.
YN330111 CU-CPT-8m 125079-83-6
CU-CPT-8m is a specificTLR8antagonist, with an IC50 of 67nM.
YN251310 Cefixime trihydrate 125110-14-7
Cefixime trihydrate (FR-17027 trihydrate) is an antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections.
YN373992 5-Lipoxygenase-In-1 125235-15-6
5-Lipoxygenase-In-1 is a5-Lipoxygenaseinhibitor extracted from patent EP 331232 A2, table 4, compound example 4.10.
YN1710016 Tr-PEG4-OH 125274-16-0
Tr-PEG4-OH is a non-cleavable 4 unit PEGADClinker used in the synthesis of antibody-drug conjugates (ADCs).
YN321701 Bepotastine 125602-71-3
Bepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor that is indicated in allergic rhinitis, urticaria, and pruritus associated with skin disease.
YN320934 Tipelukast 125961-82-2
Tipelukast (KCA 757) is a sulfidopeptideleukotriene receptorantagonist, an orally bioavailable anti-inflammatory agent and used for the treatment of asthma.
YN370209 Atorvastatin lactone 125995-03-1
Atorvastatin lactone is a prodrug form of atorvastatin. Atorvastatin is an orally active3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA)reductase inhibitor.
YN482503 Siamenoside I 126105-12-2
Siamenoside I is one of the mogrosides that has several kinds of bioactivities.
YN251672 Ginsenoside Rg4 126223-28-7
Ginsenoside Rg4 is a major protopanaxatriol type ginsenoside isolated from the leaves ofPanax ginsengC. A. Meyer. The protopanaxatriol type ginsenosides (such as Ginsenoside Rg4) exhibits various biological activities including ant...
YN360365 (R)-(+)-Anatabine 126454-22-6
(R)-(+)-Anatabine is an less active R-enantiomer of Anatabine. Anatabine is a potentα4β2 nAChRagonist. Anatabine inhibitsNF-κBactivation loweramyloid-β (Aβ)production by preventing the β-cleavage of amyloid precursor prot...
YN321546 Ciclesonide 126544-47-6
Ciclesonide is a glucocorticoid used to treat obstructive airway diseases.
KT5823, a selective the cGMP-dependent protein kinase (PKG) inhibitor with anKivalue of 0.23μM, it also inhibits PKA and PKC with Ki values of 10μM and 4μM, respectively. KT5823 is a staurosporine-related protei...
YN373496 N-Acetyl-Ser-Asp-Lys-Pro 127103-11-1
N-Acetyl-Ser-Asp-Lys-Pro, an endogenous tetrapeptide secreted by bone marrow, is a specific substrate for the N-terminal site ofACE.
YN330656 Chitohexaose hexahydrochlorid... 127171-88-4
Chitohexaose hexahydrochloride is a chitosan oligosaccharide with anti-inflammatory effect. Chitohexaose hexahydrochloride binds to the active sites ofTLR4 and inhibits LPS induced inflammation.
YN330657 Chitoheptaose heptahydrochlor... 127171-89-5
Chitoheptaose heptahydrochloride is a chitosan oligosaccharide with antioxidant, anti-inflammatory, antiapoptotic and cardioprotective activities. Chitoheptaose heptahydrochloride significantly enhances the growth and photosynthesis p...
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