Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN482970 Camelliaside B 131573-90-5
Camelliaside B is a flavonoid from the methanol extract of tea (Camellia oleifera) seed pomace.
E-6123 is a platelet-activating factor (PAF) receptor antagonist.
YM-264 is a selective, potent and orally activeplatelet-activating factor (PAF)antagonist with a pKi value of 8.85 for rabbit platelet membranes.
YN484132 Influenza HA (110-119) 132031-50-6
Influenza HA (110-119) is the 110-119 fragment of influenza virus hemagglutinin that can stimulate Treg cells proliferation.
YN320801 SR-31747 free base 132173-06-9
SR-31747 free base is asigmalig and with immunosuppressive and anti-inflammatory properties. SR-31747 blocks cell proliferation by inhibiting sterol isomerase.
SR-31747 is asigmalig and with immunosuppressive and anti-inflammatory properties. SR-31747 blocks cell proliferation by inhibiting sterol isomerase.
YN321294 Alosetron (Hydrochloride(1:X... 132414-02-9
Alosetron (GR 68755) Hydrochloride(1:X) is a potent and highly selective serotonin5-HT3 receptorantagonist. Alosetron Hydrochloride(1:X) is used for the research of irritable bowel syndrome (IBS). Alosetron Hydrochloride(1:...
NOD-IN-1 (MDK19922, Compound 4) is a potent mixed inhibitor of nucleotide-binding oligomerization domain (NOD)-like receptor 1 (NOD1) and NOD2 with IC50 of 5.74 μM and 6.45 μM, respectively.
YN483918 Osteogenic Growth Peptide, ... 132996-61-3
Osteogenic Growth Peptide, OGP is a short, naturally occurring 14-mer growth factor peptide found in serum atμM concentrations.
YN322060 LTB4-IN-1 133012-00-7
LTB4-IN-1 (Compound 6) is aleukotriene synthesis(LTB4) inhibitor with an IC50 of 70nM.
YN250139 Peldesine 133432-71-0
Peldesine (BCX 34) is a potent, competitive, reversible and orally activepurine nucleoside phosphorylase (PNP)inhibitor with IC50s of 36nM, 5nM, and 32nM forhuman, rat, and mouse red blood cell (RBC) PNP, respectivel...
YN260050 Tr-PEG3-OH 133699-09-9
Tr-PEG3-OH is a non-cleavable 3 unit PEGADClinker used in the synthesis of antibody-drug conjugates (ADCs).
YN371789 Epoxomicin 134381-21-8
Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhibits primarily the CH-L activity of the 20S proteasome, while T-L and PGPH catalytic activities are also inhibited at 100- and 1000-fold reduced ...
YN372824 Atorvastatin 134523-00-5
Atorvastatin is an orally activeHMG-CoAreductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion with IC50s of 0.39μM and 2.39μM, respectiv...
YN372431 Atorvastatin hemicalcium salt 134523-03-8
Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of cholesterol.
ONO4057 is aLeukotriene B4receptorantagonist, with an IC50 of 0.7±0.3μM.
YN330040 COX-2-IN-2 134729-13-8
COX-2-IN-2 is a selective and inducibleCOX2inhibitor with an IC50 of 0.24μM. COX-2-IN-1 is an anti-inflammatory compound with anti-inflammatory and analgesic activities.
YN482310 Fluorescein Biotin 134759-22-1
Fluorescein Biotin is used as an alternative to radioactive biotin for detecting and quantitating biotin-binding sites by either fluorescence or absorbance; the the fluorescence or absorbance of Fluorescein Biotin is quenched, upon bi...
YN482943 Camelliaside A 135095-52-2
Camelliaside A is a flavonoid from the methanol extract of tea (Camellia oleifera) seed pomace.
Arazine (N-Acetyl-S-farnesyl-L-cysteine) is a cell-permeable modulator ofG protein and G-protein coupled receptorsignaling. Arazine can be a a substrate for isoprenylcysteine methyltransferase by competing with prenylated G prote...
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