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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-1149 | M2698 CAS No.1379545-95-5 | M2698 (MSC2363318A)/CAS No.1379545-95-5 is an orally active, ATP competitive, selective p70S6K and Akt dual-inhibitor with IC50s of 1 nM for p70S6K, Akt1 and Akt3. M2698 can cross the blood-brain barrier and has anti-cancer activity. | price> |
| R-PL-0111 | PLA-PEG-Silane | Poly(D,L-lactide)-polyethylene glycol--Silane,PLA-PEG-Silane from ruixi Poly(D,L-lactide)-polyethylene glycol--Silane (PLA-PEG-Silane) is a linear A-B-C type amphiphilic triblock copolymers. It can be used in preparation of hydrogel for drug encapsulation and drug delivery. | price> |
| R-NH-001 | 5-Aminofluorescein | Protein fluorescent labeling reagent.Fluorescent antibody technology for rapid identification of pathogens. | price> |
| R-DS-0056 | DSPE-PEG-T7(HAIYPRH) | T7(HAIYPRH) is a short peptide screened by phage display technology,which can specifically bind to TfR with a binding constant as high as 10 nmol·L −1. Moreover,due to the different binding sites,endogenous TF will not inhibit, but will promote the binding of T7 modified nanoparticles to TfR.Therefore,T7 is more suitable as a target molecule,and there are many reports on the application of T7 peptide alone. | price> |
| R-R-1150 | Afuresertib hydrochloride CAS No.1047645-82-8 | Afuresertib hydrochloride (GSK 2110183 hydrochloride)/CAS No.1047645-82-8 is an orally bioavailable, selective, ATP-competitive and potent pan-Akt kinase inhibitor with Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively. | price> |
| R-PL-0112 | PLA-PEG-ACRL | Poly(D,L-lactide)-polyethylene glycol--Acrylates,PLA-PEG- ACRL from ruixi Poly(D,L-lactide)-polyethylene glycol--Acrylates (PLA-PEG- ACRL) is a linear A-B-C type amphiphilic triblock copolymers. It can be used in preparation of hydrogel for drug encapsulation and drug delivery. | price> |
| QY-C-1014 | FITC-PNA | Peanut agglutinin FITC conjugate (pna-fitc)/FITC-Peanut agglutinin was prepared by chemical cross-linking method with peanut agglutinin (PNA) and fluorescein isothiocyanate (FITC) purified by affinity chromatography.The product is soluble in PBS (pH 7.3),protein concentration≥1 mg/ml,and contains stabilizer.It can be used for PNA immunofluorescence detection,flow cytometry, analysis of interaction between biological macromolecules and research of targeted drugs. | price> |
| R-DS-0057 | DSPE-PEG-R9 | Cell penetrating peptide (CPP) is a kind of short peptide with strong penetration effect on cell membrane,which can promote cell uptake.Liposome modified by CPP can improve the rate of liposome entry into the cell,which is a new direction of targeted drug delivery carrier research. | price> |
| R-R-1151 | Cenisertib CAS No.871357-89-0 | Cenisertib (AS-703569)/CAS No.871357-89-0 is an ATP-competitive multi-kinase inhibitor that blocks the activity of Aurora-kinase-A/B, ABL1, AKT, STAT5 and FLT3. Cenisertib induces major growth-inhibitory effects by blocking the activity of several different molecular targets in neoplastic mast cells (MC). Cenisertib inhibits tumor growth in xenograft models of pancreatic, breast, colon, ovarian, and lung tumors and leukemia. | price> |
| R-PL-0113 | PLA-PEG- LA | Poly(D,L-lactide)-polyethylene glycol--Lipoic acid, PLA-PEG- LA from ruixi Poly(D,L-lactide)-polyethylene glycol--Acrylates (PLA-PEG- ACRL) is a linear A-B-C type amphiphilic triblock copolymers. It can be used in preparation of hydrogel for drug encapsulation and drug delivery. | price> |
| QY-C-1113 | FITC-SBA | Soybean agglutinin is one of the main antinutritional factors in soybean, which has a certain inhibitory effect on animal growth.Its content is an important index to evaluate the quality of animal feed.Soybean agglutinin (SBA) mainly exists in the protein bodies of soybean cotyledon cells,which is about 10% of the total soybean protein.The molecular weight of soybean lectin is about 120 kDa.It is one of the main anti nutritional factors in soybean. | price> |
| R-DS-0058 | DSPE-PEG-ADH1 | Liposomes can passively enter tumor tissue through enhanced retention and retention effect(EPR).Compared with radiotherapy and chemotherapy alone, liposomes have certain clinical treatment advantages.However,the liposome can not reach the target site immediately after injection and stay at the tumor site for a long time. | price> |
| R-R-1152 | PI3K/AKT-IN-1 | PI3K/AKT-IN-1 is an effective PI3K/AKT dual inhibitor (IC50 of 6.99, 4.01 and 3.36 μM for PI3Kγ, PI3Kδ and AKT, respectively). PI3K/AKT-IN-1 has anticancer activity and acts by inhibiting PI3K/AKT axis and inducing caspase 3 dependent apoptosis. | price> |
| R-PL-0114 | PLA-PEG-Tosyl | Poly(D,L-lactide)-polyethylene glycol--Tosylate PLA-PEG-Tosyl from ruixi Poly(D,L-lactide)-polyethylene glycol--Tosylate(PLA-PEG-Tosylate) is a linear A-B-C type amphiphilic triblock copolymers. It can be used in preparation of hydrogel for drug encapsulation and drug delivery. | price> |
| R-HPPH-1 | HPPH | HPPH (photochlor) is a second generation photosensitizer used in photodynamic therapy (PDT). | price> |
| R-DS-0059 | DSPE-PEG3400-SPA | Peptide is a compound formed by α-amino acids linked together by peptide bond, which is the intermediate product of protein hydrolysis.Peptides are widely used in medical research,drug release,nanotechnology and new materials research,cell culture.And the active compounds such as ligand research,peptide synthesis support,graft polymer,new materials and polyethylene glycol modified functional coating. | price> |
| R-R-1153 | 3CAI CAS No.28755-03-5 | 3CAI/CAS No.28755-03-5 is a potent and specific AKT1 and AKT2 inhibitor. | price> |
| R-PL-0115 | PLA-PEG-Acetylthio | Poly(D,L-lactide)-polyethylene glycol--Acetylthio,PLA-PEG-Acetylthio from ruixi Poly(D,L-lactide)-polyethylene glycol--Acetylthio (PLA-PEG-Acetylthio ) is a linear A-B-C type amphiphilic triblock copolymers. It can be used in preparation of hydrogel for drug encapsulation and drug delivery. | price> |
| R-TH-001 | 4-thiouridine | 4-thiouridine is a photoreactive (cross-linked) uridine analogue,which can be incorporated into RNA structure after phosphorylation to form 4-thioutp.4-thiouridine can be used to study the specificity and kinetics of uridine cytidine kinase. | price> |
| R-DS-0060 | PH1-PEG-DSPE | To verify the potential of targeting distribution of peptide guided liposome drug delivery system,the peptide can be coupled to the polyethylene glycol end of DSPE-PEG through the specific reaction between the sparse group and the maleimide group through the linker SPDP,and the linked products were analyzed by HPLC. We used post insertion technique to combine ph1-peg-dspe micelles with liposomes( HSPC:Chol Methods:DSPE-PEG=2:1:0.1) were co incubated to prepare targeted liposomes.However,the expression of phe2 in tumor cells was higher by Lipofectamine conjugation and liposome conjugation.Ph1 coupled with cisplatin loaded long circulating liposomes can greatly improve the cytotoxicity of cisplatin liposomes to Tie2 positive cells. | price> |

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