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Home > Products
| Cat.No. | Product name | Product Description |
| R2101221 | BI-1467335 HCl | BI-1467335, also known as PXS-4728A, is a SSAO/VAP inhibitor potentially for the |
| R2101222 | Vicriviroc Malate(maleate) | Vicriviroc maleate(Sch-417690) is a piperazine-based CCR5 receptor antagonist wi |
| R2101223 | Givinostat(free base) | Givinostat or gavinostat, aslo known as ITF2357, is a potent and orally active h |
| R2101224 | WYE-687 | WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM; |
| R2101225 | TAK-220 | TAK-220 is a selective and orally bioavailable CCR5 antagonist (IC50s: 3.5 nM an |
| R2101226 | SEL120 | SEL120-34A is a selective, orally available, and ATP-competitive CDK8 inhibitor |
| R2101227 | Olinciguat | Olinciguat is an oral guanylate cyclase (sGC) stimulator. It also has concentrat |
| R2101228 | Vicriviroc Malate | Vicriviroc has a higher binding affinity to CCR5 as opposed to SCH-C in competit |
| R2101229 | STING agonist-4 | STING agonist-4 is an agonist of stimulator of Interferon Genes (STING) receptor |
| R2101230 | WAY-600 | WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 o |
| R2101231 | BGT226 maleate (NVP-BGT226 maleate) | BGT226 (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/3 |
| R2101232 | Arginase inhibitor 1 | Arginase inhibitor 1 is a potent inhibitor of human arginases I and II (IC50s: 2 |
| R2101233 | acivicin；AT-125; U-42126 | Acivicin (AT-125), a natural product produced by Streptomyces sviceus, is a γ−gl |
| R2101234 | Cenicriviroc(mesylate) | Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 a |
| R2101235 | AZD4573 | AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enable |
| R2101236 | WYE-354 | WYE-354(IC50=5 nM) is an effective, selective and ATP-competitive mTOR inhibitor |
| R2101237 | ML-SA1 | activator of TRPML channels. |
| R2101238 | Fezolinetant | Fezolinetant is an antagonist of the neurokinin 3 receptor (NK3R). It is used fo |
| R2101239 | AZD-4320 | AZD4320 is an inhibitor of BH3-mimicking dual BCL2/BCLxL. For KPUM-MS3, KPUM-UH1 |
| R2101240 | RTA 405 | CDDO-EA is an activator of NF-E2 related factor 2/antioxidant response element ( |
| R2101241 | BDTX-189 | BDTX-189 is an orally bioavailable, irreversible, selective, small-molecule inhi |
| R2101242 | E3 Ligase Ligand-Linker Conjugates 2 | E3 Ligase Ligand-Linker Conjugates 2 is a synthesized E3 ligase ligand-linker co |
| R2101243 | E3 ligase Ligand-Linker Conjugates 28 | (S,R,S)-AHPC-C4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conju |
| R2101244 | E3 Ligase Ligand-Linker Conjugates 20 | Thalidomide-O-amido-C8-NH2 (Cereblon Ligand-Linker Conjugates 2), a synthesized |
| R2101245 | E3 ligase Ligand-Linker Conjugates 7 | (S,R,S)-AHPC-PEG4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker con |
