Home > Keywords > 
Catalog name Description price
R-CG-079 PLA-thioketal(TK)-PEG-OH Poly(D,L-lactide)-Hydrazone(Hyd)-poly(ethylene glycol)-hydroxyl,PLA-TK-PEG-OH from ruixi.thioketal(TK) has the characteristics of active oxygen reaction. In ROS environment, the chemical bond of keto mercaptan breaks, forming ketone and mercaptan, realizing drug release. As the final product, PLA-thioketal(TK)-PEG-OH has ROS response characteristics, so as to realize the drug delivery system. price>
R-R-1909 Oligomycin B CAS No.11050-94-5 Oligomycin B/CAS No.11050-94-5 is an antibiotic isolated from marine Streptomyces, used as an eukaryotic ATP synthase inhibitor, induces apoptosis. price>
R-CG-080 PLA-thioketal(TK)-PEG-CHO Poly(D,L-lactide)-Hydrazone(Hyd)-poly(ethylene glycol)-CHO,PLA-TK-PEG-CHO from ruixi.thioketal(TK) has the characteristics of active oxygen reaction. In ROS environment, the chemical bond of keto mercaptan breaks, forming ketone and mercaptan, realizing drug release. As the final product, PLA-thioketal(TK)-PEG-CHO has ROS response characteristics, so as to realize the drug delivery system. price>
R-M-761 Crustacean Erythrophore Concentrating Hormone Crustacean erythrophore concentrating hormone, pELNFSPGWamide, is also called red pigment concentrating hormone (RPCH). This crustacean hormone, which was first isolated from the eyestalk of the pink shrimp Pandalus borealis, has been detected in many decapod species. price>
R-R-1910 Pimpinellin CAS No.131-12-4 Pimpinellin/CAS No.131-12-4 is a constituent of Cyrtomium fortumei (J.). Pimpinellin inhibits the growth of tumor cells via the induction of tumor cell apoptosis. price>
R-CG-081 PLA-thioketal(TK)-PEG-fitc Poly(D,L-lactide)-Hydrazone(Hyd)-poly(ethylene glycol)-CHO,PLA-TK-PEG-CHO from ruixi.thioketal(TK) has the characteristics of active oxygen reaction. In ROS environment, the chemical bond of keto mercaptan breaks, forming ketone and mercaptan, realizing drug release. As the final product, PLA-thioketal(TK)-PEG-CHO has ROS response characteristics, so as to realize the drug delivery system. price>
R-M-762 N-2-Cyanoethyl-Val-Leu-anilide N-2-Cyanoethyl-Val-Leu-anilide,CAS :94351-52-5 from ruixi.It is a synthetic peptide. price>
R-R-1911 6-Hydroxykaempferol 3-O-β-D-glucoside CAS No.145134-61-8 6-Hydroxykaempferol 3-O-β-D-glucoside/CAS No.145134-61-8 possesses anticancer activity and induces apoptosis. price>
R-CG-082 PLA-thioketal(TK)-PEG-Rhodamine B(RhB) Poly(D,L-lactide)-Hydrazone(Hyd)-poly(ethylene glycol)-Rhodamine B(RhB),PLA-TK-PEG-Rhodamine B(RhB) from ruixi.thioketal(TK) has the characteristics of active oxygen reaction.In ROS environment, the chemical bond of keto mercaptan breaks, forming ketone and mercaptan, realizing drug release. As the final product, PLA-thioketal(TK)-PEG-Rhodamine B(RhB) has ROS response characteristics, so as to realize the drug delivery system. price>
R-M-763 Dansyl-Ala-Arg-OH trifluoroacetate salt Dansyl-Ala-Arg-OH trifluoroacetate salt is a Fluorescent substrate for carboxypeptidase M. Because the substrate and the cleavage product Dansyl-Ala-OH are equally fluorescent, the product has to be extracted with chloroform. price>
R-R-1912 (R)-CR8 trihydrochloride CAS No.1786438-30-9 (R)-CR8 (CR8) trihydrochloride/CAS No.1786438-30-9, a second-generation analog of Roscovitine, is a potent CDK1/2/5/7/9 inhibitor. (R)-CR8 trihydrochloride inhibits CDK1/cyclin B (IC50=0.09 μM), CDK2/cyclin A (0.072 μM), CDK2/cyclin E (0.041 μM), CDK5/p25 (0.11 μM), CDK7/cyclin H (1.1 μM), CDK9/cyclin T (0.18 μM) and CK1δ/ε (0.4 μM). (R)-CR8 trihydrochloride induces apoptosis and has neuroprotective effect. (R)-CR8 trihydrochloride acts as a molecular glue degrader that depletes cyclin K. price>
R-CG-083 Silica coated mesoporous Fe3O4 Mesoporous materials are conducive to the storage and control of drug release, and can achieve targeted drug release. Ferric oxide (Fe_ 3O_ 4) It is the only metal oxide approved by FDA for biomedical application. Using mesoporous Fe_ 3O_ Magnetic nanoparticles are used as drug carriers to load drug mesoporous Fe by applying an external magnetic field_ 3O_ Nanoparticles can selectively act on specific physiological parts, organs, tissues or cells, and exert drug efficacy in these parts, so as to reduce the dosage and "burst release" of drugs, improve the efficiency of drug treatment, and reduce the toxic and side effects of drugs. price>
R-M-764 Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt Highly sensitive fluorescence resonance energy transfer (FRET) substrate for neutral endopeptidase (NEP or neprilysin EC 3.4.24.11) (Km = 45 μM, kcat = 59 min⁻¹, kcat/Km = 1.3 min⁻¹μM⁻¹). Enzymatic activity can be monitored with an excitation wavelength of 342 nm and an emission wavelength of 562 nm. price>
R-R-1913 AZD5582 dihydrochloride CAS No.1883545-51-4 AZD5582 dihydrochloride/CAS No.1883545-51-4 is an antagonist of the inhibitor of apoptosis proteins (IAPs), which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis. price>
R-CG-084 peg coated mesoporous Fe3O4 poly(ethylene glycol) coated mesoporous Fe3O4,peg coated mesoporous Fe3O4 from ruixi.Mesoporous materials are conducive to the storage and control of drug release, and can achieve targeted drug release. Ferric oxide (Fe_ 3O_ 4) It is the only metal oxide approved by FDA for biomedical application. Using mesoporous Fe_ 3O_ Magnetic nanoparticles are used as drug carriers to load drug mesoporous Fe by applying an external magnetic field_ 3O_ Nanoparticles can selectively act on specific physiological parts, organs, tissues or cells, and exert drug efficacy in these parts, so as to reduce the dosage and "burst release" of drugs, improve the efficiency of drug treatment, and reduce the toxic and side effects of drugs price>
R-M-765 Calcitonin (8-32) (salmon I) trifluoroacetate salt Calcitonin (8-32) (salmon I) has been been proposed as an amylin receptor antagonist which is highly selective for amylin. sCT 8-32 reverses the inhibitory effect of amylin on glucose-induced insulin release and potentiates the insulin response to glucose in the rat perfused pancreas. price>
R-R-1914 12-HETE CAS No.71030-37-0 12-HETE/CAS No.71030-37-0, a major metabolic product of arachidonic acid using 12-LOX catalysis, inhibits cell apoptosis in a dose-dependent manner. 12-HETE promotes the activation and nuclear translocation of NF-κB through the integrin-linked kinase (ILK) pathway.12-HETE has both anti-thrombotic and pro-thrombotic effects. 12-HETE is a neuromodulator. price>
R-CG-085 peg-NH2 coated mesoporous Fe3O4,Amine(NH2)function peg-NH2 coated mesoporous Fe3O4,Amine(NH2)function,peg-NH2 coated mesoporous Fe3O4,Amine(NH2)function from ruixi.Mesoporous materials are conducive to the storage and control of drug release, and can achieve targeted drug release. Ferric oxide (Fe_ 3O_ 4) It is the only metal oxide approved by FDA for biomedical application. Using mesoporous Fe_ 3O_ Magnetic nanoparticles are used as drug carriers to load drug mesoporous Fe by applying an external magnetic field_ 3O_ Nanoparticles can selectively act on specific physiological parts, organs, tissues or cells, and exert drug efficacy in these parts, so as to reduce the dosage and "burst release" of drugs, improve the efficiency of drug treatment, and reduce the toxic and side effects of drugs. price>
R-M-766 Calcitonin C-Terminal Flanking Peptide (human) trifluoroacetate salt Calcitonin C-Terminal Flanking Peptide (human) trifluoroacetate salt,Katacalcin is a potent plasma calcium-lowering peptide, also called C-procalcitonin or PDN-21, flanks calcitonin on the C-terminal side within the human calcitonin precursor. Katacalcin specifically binds to the calcitonin receptor of CD14⁺ peripheral blood mononuclear cells. price>
R-R-1915 Apostatin-1 CAS No.2559703-06-7 Apostatin-1 (Apt-1)/CAS No.2559703-06-7 is a potent TRADD inhibitor. Apostatin-1 can bind with TRADD-N (KD=2.17 μM), disrupting its binding to both TRADD-C and TRAF2. Apostatin-1 modulates the ubiquitination of RIPK1 and beclin 1. Apostatin-1 blocks apoptosis and restores cellular homeostasis by activating autophagy in cells with accumulated mutant tau, α-synuclein, or huntingtin. price>