Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320017 SAR-100842 1195941-38-8
SAR-100842 is a lysophaphatidic acid 1 (LPA1/Edg-2) receptor inhibitor.
YN483106 4''-methyloxy-Daidzin 1195968-02-5
4''-methyloxy-Daidzin (Daidzein 7-O-Β-D-glucoside 4''-O-methylate), an isoflavone methyl-glycoside, is isolated fromCordyceps militarisgrown on germinated soybeans. Isoflavones possess immunomodulating and antiallergic activities.
YN321043 Fiboflapon sodium 1196070-26-4
Fiboflapon sodium (GSK2190915; AM-803) is a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9nM in FLAP binding, an IC50 of 76nM for inhibition ofLTB4in human bloo...
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
AZD7594 is a potent selective nonsteroidalglucocorticoid receptormodulator, with an IC50 of 0.9nM.
YN250130 Vapendavir diphosphate 1198151-75-5
Vapendavir diphosphate (BTA798 diphosphate) is a potententeroviralcapsid binder (CB). Vapendavir diphosphate (BTA798 diphosphate) possesses potent antiviral activity for enterovirus 71 (EV71) replication, withEC50values of 0.5...
YN360605 Esomeprazole magnesium salt 1198768-91-0
Esomeprazole magnesium salt ((S)-Omeprazole magnesium salt) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of theH+, K+-ATPasein gastric parietal cells. Esomeprazole magnesium ...
YN450040 β-catenin/CBP-IN-1 1198780-38-9
β-catenin/CBP-IN-1 is a potent and selectiveCBP/β-cateninantagonist, extracted from the patent WO2014092154A1. β-catenin/CBP-IN-1 has the potential for the study of liver fibrosis induced by hepatitis virus.
YN250957 Amphotericin B trihydrate 1202017-46-6
Amphotericin B trihydrate, a polyene antibiotic, is first isolated from fermenter cultures ofStreptomyces nodosus. Amphotericin B trihydrate also possesses antileishmanial activity.
GPP78 (CAY10618) is a potentNamptinhibitor with an IC50 of 3.0nM fornicotinamide adenine dinucleotide (NAD) depletion. GPP78 is cytotoxic to neuroblastoma cell line SH-SY5Y cells with an IC50 of 3.8nM by inducingauto...
B022 is a potent and selectiveNF-κB-inducing kinase (NIK)inhibitor with a Ki of 4.2nM. B022 protects liver from toxin-induced inflammation, oxidative stress, and injury.
YN372330 Epacadostat 1204669-58-8
Epacadostat (INCB024360) is a potent and selective indoleamine 2,3-dioxygenase (IDO1) inhibitor with IC50 of 10 nM and displays high selectivity over other related enzymes such as IDO2 or tryptophan 2,3-dioxygenase (TDO).
SRT3109 is an antagonist ofCXCR2, with apIC50 of 8.2, and used in the research of chemokine mediated diseases.
SRT3190 is an antagonist ofCXCR2, used in the research of chemokine mediated diseases.
YN320643 Etrasimod 1206123-37-6
Etrasimod (APD334) is a potent, selective and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor with an IC50 value of 1.88nM in CHO cells.
YN340194 Solcitinib 1206163-45-2
Solcitinib is an inhibitor of JAK1 with an IC50 of 8-9 nM, and shows 11-, 55- and 23-fold selectivity over JAK2, JAK3 and TYK2, respectively.
AM679 is a potent and selective FLAP inhibitor with IC50s of 2.2nM/0.6nM/154nM for FLAP binding/hLA/hWB respectively.
YN330161 GSK2245035 1207629-49-9
GSK2245035 is a highly potent and selective intranasalToll-Like receptor 7 (TLR7)agonist with preferential Type-1 interferon (IFN)-stimulating properties. GSK2245035 haspEC50s of 9.3 and 6.5 for IFNα and TFNα....
YN380128 CaMKII-IN-1 1208123-85-6
CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63nM; significantly high selectivity against CaMKIV, MLCK, p38a, Akt1, and PKC.
YN480410 Tepilamide fumarate 1208229-58-6
Tepilamide fumarate (XP-23829) is an oral fumaric acid ester, acts as a prodrug of monomethyl fumarate, and is used in the research of moderate to severe chronic plaque psoriasis.
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