Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN1710033 UP202-56 163838-04-8
UP202-56 is an adenosine analogue, which is an adenosinergic agonist.
TAPI-1 is aTACE(ADAM17) inhibitor and blocks the shedding of several cell surface proteins. TAPI-1 is also a metalloproteinase (MMP) inhibitor.
YN373235 Phosphoramidon Disodium 164204-38-0
Phosphoramidon Disodium Salt is a metalloendopeptidase inhibitor, widely used as a biochemical tool.
YN330314 Semapimod tetrahydrochloride 164301-51-3
Semapimod tetrahydrochloride (CNI-1493), an inhibitor ofproinflammatory cytokineproduction, can inhibitTNF-α,IL-1β, and IL-6. Semapimod tetrahydrochloride inhibits TLR4 signaling (IC50≈0.3μM). Semapimod tetrahydrochl...
YN360633 Pantoprazole sodium hydrate 164579-32-2
Pantoprazole (BY10232, SKF96022) sodium hydrate (Protonix) is a potent inhibitor of H+/K(+)-ATPase with IC50 of 6.8 μM.
YN371581 Dihydro Dutasteride 164656-22-8
Dihydro Dutasteride is a metabolite of Dutasteride. Dutasteride is a potent inhibitor of both 5 alpha-reductase isozymes.
YN482904 Kukoamine B 164991-67-7
Kukoamine B is a component of Lycii Cortex, with anti-oxidant, anti-acute inflammatory and anti-diabetic properties.
YN250545 Tenofovir diphosphate 166403-66-3
Tenofovir diphosphate (TFV-DP) is a competitiveDNA polymerasesinhibitor (with respect to dATP) and a substrate of HIV type 1 (HIV-1)reverse transcriptase(RT).
AZD 4407 is a potent5-lipoxygenaseinhibitor.
YN320192 CP-96021 hydrochloride 167011-22-5
CP-96021 hydrochloride is a balanced, combined, potent and orally activeleukotriene D4 (LTD4)/platelet activating factor (PAF)receptor antagonist with Ki values of 34nM and 37nM, respectively.
SC58451 is a potent and selectiveCOX-2 inhibitor.
YN480941 Oleanolic acid hemiphthalate ... 168770-31-8
Oleanolic acid hemiphthalate disodium salt is an anti-inflammatory agent.
YN480179 Heterocyclyl carbamate deriva... 168830-01-1
Heterocyclyl carbamate derivative 1 is a heterocyclyl carbamate derivative that may be used for the research of inflammatory and neurological diseases.
SU1498, a powerful inhibitor of KDR (IC50 = 0.7 μM), stimulates accumulation of phosphorylated ERK1/2 in endothelial cells.
YN482730 Protostemotinine 169534-85-4
Protostemotinine is an alkaloid isolated from the roots and rhizomes ofStemona sessilifolia.
YN330347 Deracoxib 169590-41-4
Deracoxib is a COX-2 inhibitor with >48-fold selectivity over COX-1. It also exhibits inhibitory activity against phosphodiesterase (Ki = 3.6 μM against human PDE4D3).
YN330283 Celecoxib 169590-42-5
Celecoxib is a selective COX-2 inhibitor with IC50 of 40 nM in Sf9 cells.
YN483154 Angelol K 169736-93-0
Angelol K is a natural product from Chinese angelica.
YN320190 ReN-1869 hydrochloride 170149-76-5
ReN 1869 hydrochloride is a novel, selectivehistamine H1receptorantagonist, which demonstrates affinity to the histamine H1receptor (guinea pig brain) with Kiof 0.19±0.04μM and the non-selective σ site (guinea pig brain) with Ki...
YN270613 Infliximab 170277-31-3
Infliximab (Avakine) is a chimeric monoclonal IgG1 antibody that specifically binds toTNF-α. Infliximab prevents the interaction ofTNF-αwith TNF-α receptor (TNFR1 and TNFR2). Infliximab has the potential for auto...
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