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Catalog | name | Description | price |
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R-XASYS-00437 | SB 225002,cas:182498-32-4 | SB 225002(C13H10BrN3O4,352.1) is a selective non-peptide inhibitor of CXCR2, inhibiting IL-8 binding to CXCR2 with an IC50 value of 22 nM.SB225002 inhibits neutrophil chemotaxis in response to IL-8 in vitro (IC50 = 20 nM) and blocks neutrophil margination induced by IL-8 in vivo (IC50 = 30 nM). | price> |
R-R-0437 | Ald-Ph-amido-PEG2-C2-Pfp ester | Ald-Ph-amido-PEG2-C2-Pfp ester/CAS 2101206-60-2 is a nonclaevable 2-unit PEG linker for antibody-drug-conjugation (ADC). | price> |
RZ-150 | Hyaluronate-SS-DOX | Hyaluronate-S-S-doxorubicin,Hyaluronate-SS-DOX from ruixi.Ruixi is a well-known biotechnology company.Hyaluronate-SS-DOX is a doxorubicin linked by a disulfide bond of hyaluronic acid.We provide a variety of high-quality products,such as hyaluronic acid disulfide bond polycaprolactone,hyaluronic acid disulfide bond polylysine. | price> |
R-XASYS-00438 | RS-25344 hydrochloride,cas:152815-28-6 | RS 25344 hydrochloride(C19H14ClN5O4,411.8) is a phosphodiesterase (PDE) 4 inhibitor | price> |
R-R-0438 | Mal-PEG2-Val-Cit-amido-PAB-OH | Mal-PEG2-Val-Cit-amido-PAB-OH/CAS: 2055041-38-6/Mal-PEG2-Val-Cit-PAB-OH is a cleavable ADC linker. The Val-Cit will specifically be cleaved by Cathepsin B. As this enzyme is only present in the lysosome, the ADC payload will be released only in the cell. The maleimide group is reactive toward thiol groups between pH 6.5 to 7.5. PEG chain increases the water solubility of the compound. | price> |
RZ-151 | Hyaluronate-SS-PTX | Hyaluronate-SS-PTX,Hyaluronate-S-S-Paclitaxel from ruixi.Ruixi is a well-known biotechnology company.Hyaluronate-s-s-paclitaxel is a taxol linked by a disulfide bond of hyaluronic acid. We can also provide a variety of other high-quality products,such as hyaluronic acid disulfide bond polycaprolactone, hyaluronic acid disulfide polylysine,hyaluronic acid disulfide bond adriamycin. As a diterpenoid alkaloid with anticancer activity,paclitaxel has novel and complex chemical structure,extensive and significant biological activity,and novel and unique mechanism of action. | price> |
R-XASYS-00439 | CMP-5,cas:880813-42-3 | CMP-5(C21H21N3,315.41) is a potent and selective PRMT5 inhibitor that is inactive against PRMT1, PRMT4, and PRMT7 enzymes. CMP-5 selectively blocks S2Me-H4R3 by inhibiting PRMT5 methyltransferase activity during histone preparation. | price> |
R-R-0439 | NH2-PEG4-Lys(Boc)-NH-(m-PEG24) | NH2-PEG4-Lys(Boc)-NH-(m-PEG24) is a cleavable 28 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | price> |
RZ-152 | HA-SS-PEG | Hyaluronate-S-S-Polyethylene glycol,HA-SS-PEG from ruixi.Ruixi is a well-known biotechnology company.Our company focuses on the production and sales of scientific research level drug delivery and drug nano targeting products.At present,our products mainly include synthetic phospholipids,PEG derivatives,block copolymers,nano gold,magnetic nanoparticles,mesoporous silica, reactive fluorescent dyes,fluorescent quantum dots,click chemistry and macrocyclic ligands. | price> |
R-XASYS-00440 | FEN1-IN-4,cas:1995893-58-7 | FEN1-IN-4 (Compound 2)(C12H12N2O3,232.24) is a human flap endonuclease-1 (hFEN1) inhibitor | price> |
R-R-0440 | DBCO-(PEG2-Val-Cit-PAB)2 | DBCO-(PEG2-Val-Cit-PAB)2 is a dual cleavable ADC linker for antibody-drug conjugates (ADCs). DBCO-(PEG2-Val-Cit-PAB)2 is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. | price> |
RZ-153 | HA-SS-FITC | HA-SS-FITC,Hyaluronate-S-S-fluorescein from ruixi.Hyaluronate-s-s-fluorescein is a fluorescent labeled bisulfide hyaluronic acid.Hyaluronate is a kind of natural macromolecular acidic mucopolysaccharide with linear molecular structure, which can realize active targeted drug delivery.We can also provide a variety of other high-quality products,such as phospholipids,PEG derivatives,block copolymers, nanoparticles,microspheres and so on. | price> |
R-XASYS-00441 | PKA-IN-1,cas:179985-52-5 | 1-Acetamido-4-cyano-3-methylisoquinoline(C13H11N3O,225.25) is a selective inhibitor of PKA (cyclic AMP-dependent protein kinase). | price> |
R-R-0441 | Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA | Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA is a double claevable 3-unit and 4-unit PEG linker for antibody-agent-conjugation (ADC). Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA also is a PROTAC linker that can be used in the synthesis of PROTACs. | price> |
RZ-154 | Chitosan-SS-cRGD | Chitosan-SS-cRGD,Chitosan-S-S-cyclo(RGDyk) from ruixi.Chitosan-SS-cRGD is an active targeting chitosan modified by disulfide ring RGD peptide.Chitosan also known as deacetylated chitin,has the properties of film-forming,biodegradation, cell affinity and biological effects.Chitosan and its derivatives can be used as targeted preparation materials.There are many kinds of targeted preparations with chitosan as carrier material, mainly nanoparticles and microspheres. | price> |
R-XASYS-00442 | 1-acetyl-3,2-toluyl-5-fluorouracil,cas:71861-76-2 | 1-Acetyl-3-o-toluyl-5-fluorouracil (A-OT-Fu)(C14H11FN2O4,290.25) is a potent an antineoplastic agent. | price> |
R-R-0442 | DBCO-PEG3 acetic-EVCit-PAB | DBCO-PEG4 acetic-EVCit-PAB CAS:2253947-17-8 is a chemical compound used in bioconjugation and drug delivery research. It is a derivative of dibenzocyclooctyne (DBCO), a reactive group that can be selectively and efficiently conjugated to azides or other strained alkenes. DBCO-PEG4 acetic-EVCit-PAB contains a PEG spacer consisting of four ethylene glycol units, a maleimide group, and a p-aminobenzoic acid group (PAB), which can be used to attach the compound to proteins or peptides through the formation of stable thioether bonds. This compound is a valuable tool for the development of targeted drug delivery systems or bioconjugates for imaging, diagnosis, or therapeutic applications. | price> |
RZ-155 | Chitosan-SS-Mannose | Chitosan-SS-Mannose,Chitosan-S-S-Mannose from ruixi.Chitosan-S-S-Mannose is a disulfide linked sugar molecule.Chitosan also known as deacetylated chitin,has the properties of film-forming, biodegradation,cell affinity and biological effects.Mannose is a kind of monosaccharide as well as a kind of hexose.In the process of carbohydrate metabolism, mannose-6-phosphate is formed by phosphorylation of hexokinase. | price> |
R-XASYS-00443 | 1-Azakenpaullone,cas:676596-65-9 | 1-Azakenpaullone(C15H10BrN3O,328.2) is an analog of kenpaullone that inhibits glycogen synthase kinase 3β (GSK3β) more potently (IC50 = 18 nM) than CDK1/cyclin B or CDK5/p25 (IC50s = 2.0 and 4.2 µM, respectively). | price> |
R-R-0443 | Gly-Gly-Gly-PEG3-TCO | Gly-Gly-Gly-Gly-PEG3-TCO/CAS: 2353409-81-9 is a PEG linked peptide that belongs to the family of PEG products. It is a TCO PEG compound that is used for the synthesis of pegylated peptides. This compound serves as a protective agent for peptides, allowing for enhanced stability and prolonged activity in various applications. | price> |